- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 17.08.2023
- Impfdatum
- 14.08.2021
- Beginn
- 22.09.2022
- Tage bis Beginn
- 404,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Antiphospholipid syndrome
Cerebrovascular accident
Symptomtext
I have now been diagnosed with Antiphospholipid syndrome. I have been a vegetarian for 35 + years and have never been sick until having had the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 1,0
- Labordaten
- I am under the care of a hematologist and neurologist. I went to Hospital ER on 9/17/22 was diagnosed with CVA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- levothyroxine vitamin D
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 16.08.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 138,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
COVID-19
COVID-19 pneumonia
Cholecystitis acute
Computerised tomogram abnormal
Cough
Death
Diarrhoea
Hypophagia
Oropharyngeal pain
SARS-CoV-2 test positive
Vomiting
Symptomtext
pt presented to ED with generalized weakness, diarrhea, vomiting, poor oral intake, mild cough, sore throat; CT scan showed acute cholecystitis; positive COVID test; COVID pneumonia; started on ABX, steroids, O2 supplementation; pt improved and was able to be sent home; she passed away at home; death certificate and med records sent to info@vaers.org per VAERS request
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 04.08.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 148,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute kidney injury
Acute respiratory failure
Ascites
Asthenia
Blood calcium increased
Blood creatinine increased
Blood magnesium decreased
Blood parathyroid hormone normal
COVID-19
Calcium ionised increased
Carbohydrate antigen 27.29
Carcinoembryonic antigen normal
Cholelithiasis
Coccydynia
Computerised tomogram abdomen abnormal
Computerised tomogram thorax abnormal
Condition aggravated
Cough
Symptomtext
12/29 To ED with lightheadedness and dizziness. Started yesterday. She has not passed out. She told the nurse she's been having black stools. She reports cough and shortness of breath. She states she had mechanical fall week ago and still has some pain in her tailbone. 12/30 COVID + Test. Decadron started. Dx with Acute hypoxic respiratory failure secondary to COVID. 1/3 Progressed well, discharged home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- See above.
- Aktuelle Erkrankungen
- Admission 7/13 - 7/19: This is a pleasant 59-year-old female who came to the ER with complaints of leg pain as well as swelling. The workup in the ER showed that she had high calcium levels. Her calcium was high at 13.8, and ionized calcium was 6.94. Magnesium was very low at 1.1. She also had acute kidney injury with a creatinine of 2.1. She does have a history of stage III CKD. CT of the abdomen and pelvis showed small volume ascites with cholelithiasis, but nothing acute. CT chest was stable from before with spiculated nodules as well as mediastinal and hilar lymphadenopathy. She was admitted and nephrology consultation was obtained. She was started on aggressive hydration and the workup for hypercalcemia was ordered. Her PTH intact was normal. Her malignancy workup included a CA 27.29 and CEA, which were all normal. She had a high kappa and lambda immunoglobulins, so Hematology consultation was obtained. Protein electrophoresis also came back normal. She was given a dose of Zometa with improvement in her calcium levels. She also had low magnesium levels, which were replaced. She was found to have iron deficiency anemia. She was started on Venofer injections. Hemoglobin remained stable with no evidence of bleeding. Renal function improved with IV fluids. Pulmonology consultation was obtained because of the spiculated nodules as well as mediastinal and hilar lymphadenopathy. It was felt that the patient had sarcoidosis, so she was started on steroids. The pulmonologist recommended steroid taper as an outpatient and follow up with her pulmonologist in the future. It was strongly emphasized to the patient that she would need malignancy workup also including mammogram, Pap smear, and also follow up on the spiculated nodules on the CT chest. She was also counseled for smoking cessation. Physical therapy evaluation was obtained because of her weakness and the recommendation is to subacute rehab, so today once arrangements are made, she could be discharged to rehab facility.
- Vorgeschichte
- Lymphadenopathy, AKI (acute kidney injury), Hypomagnesemia Essential hypertension Hypercalcemia Stage 3b chronic kidney disease History of gout Iron deficiency anemia Tobacco Use
- Andere Medikamente
- acetaminophen (TYLENOL), allopurinol (ZYLOPRIM), Ascorbic Acid 500 MG PO Tab Atenolol (TENORMIN) 100 MG PO Tab benzonatate (TESSALON) 100 MG PO Cap capsaicin (ZOSTRIX) 0.025 % EXTERNAL Cream Cholecalciferol (vitamin D) 25 MCG (1000 UT) PO T
- Allergien
- Latex, Zestril
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Pulmonary embolism
Symptomtext
PATIENT RECIEVED VACCINATION ON 1/28/22 PATIENT WENT TO HOSPITAL THE WEEKEND OF 2/5/22 AND LATER PASSED ON 2/7/22. HER FAMILY REPORT SHE PASSED AWAY FROM PULMONARY EMOBLI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UTI
- Vorgeschichte
- HIGH BLOOD PRESSURE, OBESITY, SMOKING, INSOMNIA, PAIN, GERD, HIGH CHOLESTEROL
- Andere Medikamente
- VENLAFAXINE 150MG METOPROLOL TART 25MG OMEPRAZOLE 20MG FENOFIBRATE 160MG GABAPENTIN 300MG LOSARTAN/HCTZ 100-25MG TIZANIDINE 4MG ZOLPIDEM 5MG FUROSEMIDE 40MG BUSPIRONE 15MG PROMETHAZINE 25MG MACROBID 100MG 2/1/22-2/5/22
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 08.09.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 97,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Catheterisation cardiac abnormal
Coronary arterial stent insertion
Myocardial infarction
Symptomtext
never having any heart or blood pressure problems before. on 12-14-21 I had a major heart attack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 2,0
- Labordaten
- Had catherization of heart and stent put in.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 04.10.2021
- Impfdatum
- 22.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acquired diaphragmatic eventration
Adult failure to thrive
Basophil count normal
Basophil percentage
Chest X-ray abnormal
Death
Dyspnoea
Eosinophil count normal
Eosinophil percentage
Fatigue
Haematocrit decreased
Haemoglobin decreased
Lung infiltration
Lymphocyte count decreased
Lymphocyte percentage decreased
Mean cell haemoglobin concentration normal
Mean cell haemoglobin normal
Mean cell volume normal
Symptomtext
Guest passed/expired within 10 days of dose #2 of COVID-19 vaccine series. Began transitioning on 9/27/21-- 5 days s/p Dose #2. Guest was a hospice resident prior to COVID-19 vaccine and overall was having general decline prior to vaccination. Signed on to hospice on 8/6/21. Had active diagnosis of adult failure to thrive and hx of gastric CA--declined PEG tube. Only acute side effect 2 days s/p dose 2 noted was fatigue. No side side effects were reported with dose #1.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- |AGE: 78 GENDER: M | DATE&TIME: | 07/16/21 11:49 | |RCVD: 07/16/21 | |RPTD: 07/16/21 | RM 133 R E S U L T S RBC 3.71(L) 4.10-6.20 10^6/uL HEMOGLOBIN 10.0(L) 13.5-17.5 g/dL HEMATOCRIT 29.8(L) 41.0-53.0 % MCV 80 80.0-97.0 fL MCH 27.0 26.0-32.0 pg/cell MCHC 33.6 32.0-37.0 g/dL RDW 17.9(H) 11.5-14.5 % MPV 10.3 7.5-11.2 fl PLATELET COUNT 97(L) 130-400 10^3/uL NEUTROPHIL% 81.1(H) 40.0-74.0 % LYMPHOCYTE% 11.3(L) 19.0-48.0 % MONOCYTES% 6.2 2.0-11.0 % EOSONOPHIL% 0.7 0.0-7.0 % BASOPHIL% 0.7 0.0-1.5 % NEUTROPHIL# 5.7 1.7-7.7 10^3/uL LYMPHOCYTE# 0.8(L) 1.0-4.8 10^3/uL MONOCYTE# 0.4 0.0-1.0 10^3/uL EOSINOPHIL# 0.1 0.04-0.45 10^3/uL BASOPHIL# 0.1 0.00-0.20 10^3/uL MI PRE-ALBUMIN 11(L) 17.0-34.0 mg/dL INTERPRETATION: Reason for Study: R06.02 SHORTNESS OF BREATH XRAY CHEST 1 VIEW See Note FINDINGS: The heart is normal in size and configuration. The mediastinum is normal without adenopathy. There is a minimal right lower lobe infiltrate. There is no venous congestion. The osseous structures are unremarkable. CONCLUSION: Minimal right lower lobe infiltrate . The right hemidiaphragm is elevated
- Aktuelle Erkrankungen
- Diagnoses: ANEMIA, UNSPECIFIED(D64.9), UNSPECIFIED PROTEIN-CALORIE MALNUTRITION(E46), ADULT FAILURE TO THRIVE(R62.7), PERSONAL HISTORY OF OTHER MALIGNANT NEOPLASM OF STOMACH(Z85.028), TYPE 2 DIABETES MELLITUS WITHOUT COMPLICATIONS(E11.9), ANXIETY DISORDER, UNSPECIFIED(F41.9), UNSPECIFIED FALL, SUBSEQUENT ENCOUNTER(W19.XXXD), DIAPHRAGMATIC HERNIA WITHOUT OBSTRUCTION OR GANGRENE(K44.9), DIFFICULTY IN WALKING, NOT ELSEWHERE CLASSIFIED(R26.2), MUSCLE WASTING AND ATROPHY, NOT ELSEWHERE CLASSIFIED, UNSPECIFIED SITE(M62.50), DYSPHAGIA, OROPHARYNGEAL PHASE(R13.12), LOW BACK PAIN(M54.5), IDIOPATHIC HYPOTENSION (I95.0), CONSTIPATION, UNSPECIFIED(K59.00), PRESSURE ULCER OF OTHER SITE, STAGE 1(L89.891), CHRONIC KIDNEY DISEASE, STAGE 3 UNSPECIFIED(N18.30)
- Vorgeschichte
- Diagnoses: ANEMIA, UNSPECIFIED(D64.9), UNSPECIFIED PROTEIN-CALORIE MALNUTRITION(E46), ADULT FAILURE TO THRIVE(R62.7), PERSONAL HISTORY OF OTHER MALIGNANT NEOPLASM OF STOMACH(Z85.028), TYPE 2 DIABETES MELLITUS WITHOUT COMPLICATIONS(E11.9), ANXIETY DISORDER, UNSPECIFIED(F41.9), UNSPECIFIED FALL, SUBSEQUENT ENCOUNTER(W19.XXXD), DIAPHRAGMATIC HERNIA WITHOUT OBSTRUCTION OR GANGRENE(K44.9), DIFFICULTY IN WALKING, NOT ELSEWHERE CLASSIFIED(R26.2), MUSCLE WASTING AND ATROPHY, NOT ELSEWHERE CLASSIFIED, UNSPECIFIED SITE(M62.50), DYSPHAGIA, OROPHARYNGEAL PHASE(R13.12), LOW BACK PAIN(M54.5), IDIOPATHIC HYPOTENSION (I95.0), CONSTIPATION, UNSPECIFIED(K59.00), PRESSURE ULCER OF OTHER SITE, STAGE 1(L89.891), CHRONIC KIDNEY DISEASE, STAGE 3 UNSPECIFIED(N18.30)
- Andere Medikamente
- 4 oz. house supplement with meals. Administer SARS-COV-2 (COVID-19) vaccine, mRNA, spike protein, LNP, preservative free, 100 mcg/0.5 mL dose, 2-dose vaccine (Moderna) To receive dose #1 on 8/11/21 1 Administer SARS-COV-2 (COVID-19) vacc
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 27.09.2021
- Impfdatum
- 19.07.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 31,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: ja
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Aneurysm
Death
Fall
Headache
Malaise
Symptomtext
Severe headache within 4 hours of shot and after 4 days of feeling very unwell Pt stood up and fell over instantly of and aneurysm and died .I lost my partner of 23 years due to vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Rushed to emergency hospital 9/25/2021 then air lifted to another HCF
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 25.09.2021
- Impfdatum
- 09.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 23,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac dysfunction
Cardio-respiratory arrest
Chest pain
Fatigue
Illness
Myocardial infarction
Thrombosis
Symptomtext
heart function is down to 35%; clot in heart; he started having chest pains; consumer had a heart attack, died, and "brought me back"; coded; he was sick; He states he is still tired from all the events; This spontaneous case was reported by a consumer and describes the occurrence of MYOCARDIAL INFARCTION (consumer had a heart attack, died, and "brought me back"), CARDIAC DYSFUNCTION (heart function is down to 35%), THROMBOSIS (clot in heart), ILLNESS (he was sick), CHEST PAIN (he started having chest pains), FATIGUE (He states he is still tired from all the events) and CARDIO-RESPIRATORY ARREST (coded) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 037F21A and 939902) for COVID-19 vaccination. The patient's past medical history included Thyroid disorder and Hypercholesterolemia. On 09-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 07-Sep-2021, the patient experienced ILLNESS (he was sick) (seriousness criteria hospitalization, medically significant and life threatening). On 09-Sep-2021, the patient experienced MYOCARDIAL INFARCTION (consumer had a heart attack, died, and "brought me back") (seriousness criteria hospitalization, medically significant and life threatening), THROMBOSIS (clot in heart) (seriousness criteria hospitalization, medically significant and life threatening), CHEST PAIN (he started having chest pains) (seriousness criteria hospitalization, medically significant and life threatening) and CARDIO-RESPIRATORY ARREST (coded) (seriousness criteria hospitalization, medically significant and life threatening). In September 2021, the patient experienced FATIGUE (He states he is still tired from all the events) (seriousness criteria hospitalization, medically significant and life threatening). On an unknown date, the patient experienced CARDIAC DYSFUNCTION (heart function is down to 35%) (seriousness criteria hospitalization, medically significant and life threatening). The patient was hospitalized from 09-Sep-2021 to 13-Sep-2021 due to CARDIAC DYSFUNCTION, CARDIO-RESPIRATORY ARREST, CHEST PAIN, FATIGUE, ILLNESS, MYOCARDIAL INFARCTION and THROMBOSIS. At the time of the report, MYOCARDIAL INFARCTION (consumer had a heart attack, died, and "brought me back"), CARDIAC DYSFUNCTION (heart function is down to 35%), THROMBOSIS (clot in heart), ILLNESS (he was sick), CHEST PAIN (he started having chest pains), FATIGUE (He states he is still tired from all the events) and CARDIO-RESPIRATORY ARREST (coded) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant products included thyroid and cholesterol medication. Treatment information not provided. Consumer states that 2 days after vaccination, consumer had a heart attack, died, and brought back. Consumer repeated that pattern twice heart attack, died and brought back. Consumer also reports he had clot in heart and heart function was down to 35%. Consumer states that on 07 Sep 2021 he was sick and part of 08 Sep 2021. On 09 Sep 2021, around 4:45 AM he started having chest pains and was transported to hospital via helicopter. Consumer was hospitalized from 09Sep2021 to 13Sep2021. Consumer cannot confirm for sure if any surgery was done, he mentioned might be a stent was put in. Consumer states they started 8 new pills for him including blood thinners. Company comment: This case concerns a 73 year-old male subject with no reported medical history who experienced the unexpected events of myocardial infarction, cardiac dysfunction, thrombosis, illness, chest pain, cardiopulmonary arrest, and fatigue. The events myocardial infarction, cardiac dysfunction, thrombosis, illness, chest pain, cardiopulmonary arrest occurred approximately 30 to 31 days after the second dose of mRNA-1273. The event fatigue occurred at an unknown date. The rechallenge was unknown as information on the first dose and subsequent events are not provided. The medical history hypercholesterolemia and thyroid disorder remain confounders. The benefit-risk relationship of mRNA-1273 (Spikevax) is not affected by this report.; Sender's Comments: This case concerns a 73 year-old male subject with no reported medical history who experienced the unexpected events of myocardial infarction, cardiac dysfunction, thrombosis, illness, chest pain, cardiopulmonary arrest, and fatigue. The events myocardial infarction, cardiac dysfunction, thrombosis, illness, chest pain, cardiopulmonary arrest occurred approximately 30 to 31 days after the second dose of mRNA-1273. The event fatigue occurred at an unknown date. The rechallenge was unknown as information on the first dose and subsequent events are not provided. The medical history hypercholesterolemia and thyroid disorder remain confounders. The benefit-risk relationship of mRNA-1273 (Spikevax) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypercholesterolemia; Thyroid disorder.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 21.09.2021
- Impfdatum
- 09.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Anticoagulant therapy
Asthenia
Blood test
Cardiac assistance device user
Cardiac dysfunction
Cardio-respiratory arrest
Catheterisation cardiac abnormal
Intracardiac thrombus
Myocardial infarction
Nausea
Ultrasound scan
Symptomtext
Massive heart attack after 2 days after 2nd injection. Coded twice, once on life flight and once at emergency room. Attempted to remove clot with clot buster after/during heart cath. Only have 35% heart function, feel weak, nauseous and wearing life vest defibrillator for 3 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- 6,0
- Labordaten
- Heart Cath 9/9/2021 and 9/10/2021. Blood test daily. Ultrasound on 9/11/2021 and 9/14/2021.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cholesterol & pacemaker
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 20.08.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Computerised tomogram
Electroencephalogram
Epilepsy
Generalised tonic-clonic seizure
Magnetic resonance imaging
Symptomtext
August 31st had a tonic-clonic seizure at 5:00 am, had another one on November 10th 4:30am. Due to having a second one I was diagnosed with epilepsy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- -
- Labordaten
- CAT scan, MRI, EEG
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 25.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Computerised tomogram normal
Computerised tomogram thorax normal
Dizziness
Echocardiogram normal
Fatigue
Full blood count normal
Incorrect dose administered
Loss of consciousness
Malaise
Mental impairment
Syncope
Symptomtext
When they administered the booster, they gave me a full dose not the half dose required for booster vaccine. At about 06:00PM I started not feeling well. I felt woozy, tired and was not able to think clearly. When I woke up in the morning I passed out. I was taken to the hospital in an ambulance. At the hospital they did a CT Scan of my lungs, CBC, Echocardiogram, Chest CT and they did not find anything wrong. They weren't sure if it was because I was dehydrated when I was vaccinated. I was diagnosed with Syncope and possible dehydration. I was discharged the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- 1,0
- Labordaten
- 08/26/2021: Medical Center: CT Scan: Normal; CBC: Normal; Echocardiogram: Normal; Chest CT: Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diffuse Large B-Cell Lymphoma; Asthma
- Andere Medikamente
- Crestor 5mg Once daily Loratadine 10mg once daily Lutein 20mg Once daily. Calcium with Vitamin D
- Allergien
- Penicillin
- Vorherige Impfungen
- 05/31/2019 Flu Vaccine: Was hospitalized for 4 days and was diagnosed with moderate to intermediate asthma.
- Staat
- MO
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 17.08.2021
- Beginn
- 08.02.2022
- Tage bis Beginn
- 175,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test
COVID-19
Chest X-ray
Computerised tomogram
Dyspnoea
Intensive care
Oropharyngeal pain
Pneumonia
SARS-CoV-2 test positive
Vomiting
Symptomtext
He started with a sore throat and breathing issues. He then began vomiting but never had a temperature but was getting weak so I took him to the emergency room. They indicated that he had pneumonia and verified that he had COVID. He was admitted to the ICU on 02-11-2022. He is still currently being treated. He is on prolonged isolation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 11,0
- Labordaten
- COVID test, chest x-ray, blood work, Cat Scan.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes; high blood pressure; kidney disease
- Andere Medikamente
- Myfortic; tacrolimus; allopurinol; aspirin; cilistol; clonidine; furosemide; levothyroxine; metformin; Bystolic; omeprazole; Humalog; Lantis; Lipitor; Micardis; fish oil; juice plus; Preservision
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 28.08.2021
- Beginn
- 13.09.2021
- Tage bis Beginn
- 16,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Computerised tomogram head normal
Laboratory test normal
Seizure
Symptomtext
Seizures (patient had first seizure 9/13/21 and has had two more since)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Normal labs and CT brain
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- -
- Allergien
- Ciprofloxacin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 09.11.2021
- Impfdatum
- 09.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angina pectoris
Axillary pain
Chest pain
Fatigue
Myocarditis
Symptomtext
Myocarditis symptoms, pain around my heart especially when lying down in bed. Fatigue, soreness in upper left chest and underarm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Reported to doctor and having blood work done for a plaque test
- Aktuelle Erkrankungen
- No ne
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 21.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Disturbance in attention
Dizziness
Electrocardiogram
Fatigue
Heart rate increased
Hyperhidrosis
Feeling abnormal
Myalgia
Pain
Presyncope
Tachycardia
Symptomtext
Extreme dizziness to the point of almost falling, at the same time extreme sweating, even on the back of the hands. This sweating lasted for 45 minutes to an hour. Dizziness remains a problem. Muscle aches and chills. Brain "fog" or lack of ability to concentrate or focus. This lasted for a week. Extreme tiredness lasting for a week. Increased heart rate began after 5-6 days, getting as high as 172 and combined with dizziness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- EKG performed September 27, 2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bronchiectises
- Andere Medikamente
- Olmesartan Medoxomil 20 mg 1 daily Blood pressure Hydrochlorothiazide 25 MG Tablets 1 daily Blood pressure Desvenlafaxine (Pristiq)- 25 mg? In morning Levothroid 125 MCG Flonase - Allergies Ventolin HFA 90MCG 2 puffs every 4-6 hrs as need
- Allergien
- None
- Vorherige Impfungen
- Muscle aches, chills, dizziness. 73 years old, Moderna, 01/19/2021 and Moderna, 02/17/2021
- Staat
- NC
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 21.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Disturbance in attention
Dizziness
Electrocardiogram
Fatigue
Heart rate increased
Hyperhidrosis
Feeling abnormal
Myalgia
Pain
Presyncope
Tachycardia
Symptomtext
Extreme dizziness to the point of almost falling, at the same time extreme sweating, even on the back of the hands. This sweating lasted for 45 minutes to an hour. Dizziness remains a problem. Muscle aches and chills. Brain "fog" or lack of ability to concentrate or focus. This lasted for a week. Extreme tiredness lasting for a week. Increased heart rate began after 5-6 days, getting as high as 172 and combined with dizziness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- EKG performed September 27, 2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bronchiectises
- Andere Medikamente
- Olmesartan Medoxomil 20 mg 1 daily Blood pressure Hydrochlorothiazide 25 MG Tablets 1 daily Blood pressure Desvenlafaxine (Pristiq)- 25 mg? In morning Levothroid 125 MCG Flonase - Allergies Ventolin HFA 90MCG 2 puffs every 4-6 hrs as need
- Allergien
- None
- Vorherige Impfungen
- Muscle aches, chills, dizziness. 73 years old, Moderna, 01/19/2021 and Moderna, 02/17/2021
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 04.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Chills
Confusional state
Diarrhoea
Dizziness
Fatigue
Flushing
Headache
Hyperhidrosis
Insomnia
Nausea
Pain
Palpitations
Pyrexia
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Abdominal Pain-Medium, Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, Systemic: Confusion-Medium, Systemic: Diarrhea-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fainting / Unresponsive-Severe, Systemic: Fever-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Systemic: Nausea-Medium, Systemic: Unable to Sleep-Severe, Additional Details: Severe Palpitation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 01.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anaphylactic reaction
Chest discomfort
Chest pain
Dysphagia
Dyspnoea
Headache
Intensive care
Nausea
Eye swelling
Injection site erythema
Injection site pruritus
Injection site swelling
Mouth swelling
Pruritus
Rash
Swelling face
Swollen tongue
Throat tightness
Symptomtext
Dose given at Pharmacy, developed generalized itching, urticaria, chest tightness, SOB, nausea, and frontal non-pulsatile headache, given IM epi x1. Transported to ED, received second IM epi for ongoing symptoms. Admitted to the surgical ICU for airway watch, ongoing symptoms, given third IM epi. Continued to have SOB, required an epinephrine drip to be started, also received multiple doses of solumedrol, Benadryl, inhalers, Pepcid, and required an insulin drip.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, migraines, GERD
- Andere Medikamente
- Albuterol, Symbicort, Zyrtec, Dexilant, Lexapro, motrin, lamictal, ativan
- Allergien
- Amoxicillin - hives, dyspnea Fentanyl - dyspnea Contrast - hives, dyspnea Apples, plums, cherries, bananas, watermelon - mouth itching Avocado - tongue swelling Shrimp - throat tight, dyspnea, urticaria Dust mites, dog, cat, cockroach, mold, tree pollen, grass pollen, weed pollen - +skin test
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 01.10.2021
- Impfdatum
- 31.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Asthenia
Blindness
Body temperature
Diarrhoea
Dyspnoea
Fatigue
Feeling abnormal
Pain
Palpitations
Pruritus
SARS-CoV-2 test
Syncope
Symptomtext
vision blindness, he could not see; Fainting; severe diarrhea; Did not have any strenght/lack of energy; Had real bad itching general in all the body; Heart felt like it was racing; Had real harsh breathing, was breathing real hard; Pain; He's kinda lost out, does not feel like his normal self, is like 90% normal; Had lots of anxiety; fatigued, totally fatigued; This spontaneous case was reported by a consumer and describes the occurrence of BLINDNESS (vision blindness, he could not see) and SYNCOPE (Fainting) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical reported history provided by the reporter. Concomitant products included OXYCODONE for Chronic pain, KETOPROFEN (AMAPROGEL) and IBUPROFEN for an unknown indication. On 31-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced BLINDNESS (vision blindness, he could not see) (seriousness criterion medically significant), SYNCOPE (Fainting) (seriousness criterion medically significant), DIARRHOEA (severe diarrhea), ASTHENIA (Did not have any strenght/lack of energy), PRURITUS (Had real bad itching general in all the body), PALPITATIONS (Heart felt like it was racing), DYSPNOEA (Had real harsh breathing, was breathing real hard), PAIN (Pain), FEELING ABNORMAL (He's kinda lost out, does not feel like his normal self, is like 90% normal), ANXIETY (Had lots of anxiety) and FATIGUE (fatigued, totally fatigued). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency. At the time of the report, BLINDNESS (vision blindness, he could not see), SYNCOPE (Fainting), DIARRHOEA (severe diarrhea), ASTHENIA (Did not have any strenght/lack of energy), PRURITUS (Had real bad itching general in all the body), PALPITATIONS (Heart felt like it was racing), DYSPNOEA (Had real harsh breathing, was breathing real hard), PAIN (Pain), FEELING ABNORMAL (He's kinda lost out, does not feel like his normal self, is like 90% normal), ANXIETY (Had lots of anxiety) and FATIGUE (fatigued, totally fatigued) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Body temperature: 96 (normal) 96. On 21-Aug-2021, SARS-CoV-2 test: negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Company Comment: This case concerns a 67 year old male with no relevant medical history who experienced serious unexpected events of blindess and syncope on unknown date. Patient received 1st dose of Moderna Covid 19 vaccine. Rechallenge is not applicable. The benefit-risk relationship is not affected by this report.; Sender's Comments: This case concerns a 67 year old male with no relevant medical history who experienced serious unexpected events of blindess and syncope on unknown date. Patient received 1st dose of Moderna Covid 19 vaccine. Rechallenge is not applicable. The benefit-risk relationship is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: Body Temperature; Result Unstructured Data: 96; Test Date: 20210821; Test Name: COVID test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical reported history provided by the reporter.
- Andere Medikamente
- AMAPROGEL; OXYCODONE; IBUPROFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Head injury
Hyperhidrosis
Skin abrasion
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: patient fainted and fell and scraped his face, given glucose tabs and water, become responsive seconds after falling, was sweating. Pharmacist made the patient sit for 30 minutes and patient stated feeling much better. Pharmacist walked patient to car to insure stability on feet and was okay. No other intervention was necessary. Fully recovered with minor scratches on face. Pharmacist advised patient to come accompanied for second dose and make pharmacist aware of incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 04.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: Pt had passed out after 5 mins of vaccine administration. Pt came to and ambulance was called for check up
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 11.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Dizziness
Headache
Nausea
Seizure
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Headache-Mild, Systemic: Nausea-Mild, Systemic: Seizure-Mild, Systemic: Weakness-Mild, Additional Details: patient had a seizure about 10 minutes after receiving the moderna vaccine. the seizure episode lasted 30-60 seconds. the patient regained consciousness, but experienced lightheadedness, weakness, nausea, headache, and chills. patient was provided with a benadryl 25 mg, orange juice, and a cookie. patient felt better afterward. patient will follow up with a physician at an urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 14.09.2021
- Impfdatum
- 08.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood creatinine
C-reactive protein increased
Chest X-ray
Chest discomfort
Chest pain
Differential white blood cell count
Dyspnoea
Electrocardiogram
Fibrin D dimer
Full blood count
Inflammatory marker increased
Metabolic function test
Musculoskeletal pain
Pericarditis
Red blood cell sedimentation rate increased
SARS-CoV-2 test negative
Troponin
Symptomtext
9/10/21 tightness in chest began at 12pm. Shortness of breath very mild Friday night, 9/11/21 chest tightness increasing and more shortness of breath. 9/12/21 chest pain and tightness, short of breath and sharp pain under left shoulder blade began. 9/13/21 went to ER 8am at the advice of PCP. Diagnosed with acute pericarditis. Given aspirin, Solu-medrol, nebulizer treatment, labs drawn, chest xray and ekg performed. Covid swab (negative). Sent home with prescription for anti-inflammatories, inhaler and to rest and monitor vital signs and symptoms for worsening.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- 9/13/21 EKG, chest xray, CBC w auto diff, D-Dimer quantitative, CRP elevated (1.3), Sed rate elevated (24), Creatinine, CMP, Troponin x2, covid swab inflammatory markers elevated
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Penicillin, IV contrast dye, Augmentin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 14.09.2021
- Impfdatum
- 28.08.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
Disturbance in attention
Fatigue
Gait inability
Hypoaesthesia
Blood test normal
Gait disturbance
Limb discomfort
Tremor
Lethargy
Pain
Paralysis
Syncope
Unresponsive to stimuli
Symptomtext
After the vaccine(1st One) my legs felt heavy. Five days after that, I was at work at 3PM and my legs started to tremor And then I could not walk. Feet were dragging.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- All Blood work normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None; Migraine
- Andere Medikamente
- CITALOPRAM
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 12.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Generalised tonic-clonic seizure
Headache
Symptomtext
a bad headache for 3 days; grand mal seizure; Grand mal seizure; This spontaneous case was reported by a consumer and describes the occurrence of GENERALISED TONIC-CLONIC SEIZURE (Grand mal seizure) and GENERALISED TONIC-CLONIC SEIZURE (grand mal seizure) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Seizure. Concomitant products included LACOSAMIDE (VIMPAT) and LEVETIRACETAM (KEPPRA [LEVETIRACETAM]) for an unknown indication. On 12-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Aug-2021, the patient experienced GENERALISED TONIC-CLONIC SEIZURE (Grand mal seizure) (seriousness criterion medically significant). On 01-Sep-2021, the patient experienced GENERALISED TONIC-CLONIC SEIZURE (grand mal seizure) (seriousness criterion medically significant). On an unknown date, the patient experienced HEADACHE (a bad headache for 3 days). On 19-Aug-2021, GENERALISED TONIC-CLONIC SEIZURE (Grand mal seizure) had resolved. On 01-Sep-2021, GENERALISED TONIC-CLONIC SEIZURE (grand mal seizure) had resolved. At the time of the report, HEADACHE (a bad headache for 3 days) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Treatment included use of magnet to swipe across their chest when a seizure occurs. It was reported that patient had a DNS on the left side of their chest. Lab data included Blood tests. Company comment: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, underlying medical history of seizures and use of concomitant medication are cofounder.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, underlying medical history of seizures and use of concomitant medication are cofounder.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Seizure
- Vorgeschichte
- -
- Andere Medikamente
- VIMPAT; KEPPRA [LEVETIRACETAM]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 09.09.2021
- Impfdatum
- 07.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Dizziness
Dyspnoea
Hyperhidrosis
Nodule
Pyrexia
Syncope
Symptomtext
bruising/knot in left leg. Fever, sweats. shortness of breath. fainting spells. light headed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 06.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose normal
Disorientation
Dizziness
Eye movement disorder
Fall
Feeling abnormal
Feeling hot
Flushing
Head discomfort
Loss of consciousness
Musculoskeletal stiffness
Nausea
Tremor
Vision blurred
Visual impairment
Symptomtext
21 hours after my 2nd dose while waiting in line at a restaurant i began to feel very hot. I suddenly became nauseated and dizzy. I began to feel my body stiffen and start to shake but I could not stop it. The harder I tried the worse it got, my vision became distorted and I don't remember much after that. According to witnesses I was talking during the shaking and began to fall, they helped me to the floor where my eyes rolled back in my head and I proceeded to pass out. They advised I was out for maybe 30 sec before I began to come to. I was disoriented and feeling very flushed, I felt very fuzzy and everything was in a haze. I could not move at this point. Slowly as i began to get my bearings about me i began to talk and console my mother verbally as they kept me on the ground till paramedics showed up. They advised my blood sugar was at 120 , my bp was palpable at 70 systolic. The restaurant was too loud for them to get a reg. bp. The FD and Police were on scene. This all occurred at the cafe in the mall as there were many many witnesses. I do not have ins. so I did not want to be taken to the hospital. There has been pressure in my head ever since the episode. No new meds or food has been introduced to my system. I do not have any significant medical history. None that would have caused an episode as this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Duloxetine, Valtrex, Excedrin Migraine
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 05.09.2021
- Impfdatum
- 25.08.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 10,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Venous thrombosis limb
Symptomtext
Small blood clots in veins in hands and both arms from elbows down appear reddened
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Venous thrombosis limb
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Vasculitis ,Wegeners Granulomatosis, Microscopic Ployangiitis
- Vorgeschichte
- Same as above
- Andere Medikamente
- Otrexup 12.5mg SQ weekly; Protonix; Folic Acid; Vitamion C;Carafate; Zinc; Prednisone; Xarelto 20 mg daily; lasix 40mg daily; Adderall 25mg; Plaquenil 200mg BID; Super B complex; Calcium; Vat D3; Omega 3; Ditropan Xl 5mg; Symbicort inhaler
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 29.08.2021
- Beginn
- 29.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Nausea
Pain
Pyrexia
Seizure
Vomiting
Symptomtext
Day of vaccine: fever, chills exhausted, headache, nausea and vomiting. Day after vaccine: exhausted, headache, body aches and some type of seizure. Days 2-5: body aches, headache. Saw primary medical provider and awaiting appointment with neurologist
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Being scheduled. Exact times vaccine received and onset of reactions are approximate.
- Aktuelle Erkrankungen
- COVID, pneumonia
- Vorgeschichte
- Major depression w/ anxiety, migraines, gastric bypass, restless leg syndrome
- Andere Medikamente
- Trazadone, ropinirole, Tylenol, sumatryptin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaphylactic reaction
Chest discomfort
Dysgeusia
Muscle tightness
Throat irritation
Symptomtext
Nickel taste, throat itching, mild anaphylaxis, chest tightening, upper right back tightening
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Eczema, prediabetes
- Andere Medikamente
- Montelukast SOD, Benadryl, full spectrum spearmint leaf, Ginger call Ma evening primrose, omega-3 fish oil, Loratadine
- Allergien
- Sesame seed
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 03.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Symptomtext
WITHIN 5 minutes of BoTh vaceinations , patient fainteD to flooR. RegaineD consciousness after a Few seconds (approx). patient states she Doesn't think she hit any- thing on way Down DenieD amBulance , was proviDED wateR.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.09.2021
- Impfdatum
- 27.08.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Eye contusion
Face injury
Haemorrhage
Hyperhidrosis
Insomnia
Nausea
Pain
Pyrexia
Syncope
Symptomtext
Four hours after the Modera booster, I experienced chills, body aches, fever. I went to bed but couldn't get to sleep. At 1:00 a.m., the fever was 102.6. I took 500 mg Acetaminophen and returned to bed. When the fever broke, I experienced severe sweating followed by nausea. I fainted and hit my face on the tile floor of my bathroom breaking the skin just above the right eyebrow. Within 30 minutes, that entire eye socket and surrounding area was dark purple. I was able to stop the bleeding and did not need to seek medical attention. There was no further nausea. The body aches and a lower fever (101.5) lasted throughout that day. By Sunday, I started feeling better and have improved each day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- 24 hours of body aches, chills & mild fever following 2nd Covid shot on 02/21/21 lot #022M20A
- Staat
- MN
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 30.08.2021
- Impfdatum
- 27.08.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Pallor
Symptomtext
This was second moderna dose. patient also passed out after first dose. I gave vaccine, patient seemed fine then passed out about 30 seconds later. was out for 30-40 seconds then came back to feeling very light headed and he was also very pale. I offered water and crackers. he sat with me and his mom for 20-30 minutes and was feeling fine when they left. -mom stated that his sister also reacted the same way.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- moderna 07/24/2021
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 29.08.2021
- Impfdatum
- 28.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Flushing
Hyperhidrosis
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: Shortly after receiving the moderna covid vaccine (less than 5 minutes), the patient fainted but remained breathing with a normal pulse. The patient experienced sweating and flushing. Patient flucuated between responsive and unresponsive. EMS arrived within 5 minutes of the incident to take the patient to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 27.08.2021
- Impfdatum
- 26.08.2021
- Beginn
- 26.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Confusional state
Dizziness
Dyspnoea
Hyperventilation
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hyperventilation-Severe, Systemic: Weakness-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Borrelia test
Chest pain
Chills
Dysphonia
Dyspnoea
Headache
Influenza like illness
Influenza virus test negative
Metabolic function test
Pyrexia
Respiratory tract infection viral
Rhinorrhoea
SARS-CoV-2 test negative
Sneezing
Syncope
Vaccination complication
Symptomtext
chills,syncope, blood pressure 180/110. mild fever, headache, flu like symptoms, chest pains, winded, raspy voice, sneezing, runny nose (dx by ER= viral respiratory infection but tested neg for covudand flu .. rx z pack and prednisone .. on 8/18 go to see pcp on 8/20 still having chills and symptoms my pcp said Adverse Reaction to Vaccine said i need to report . pcp advises i do not get the 2nd dose. rx potassium blood pressure medication
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- 8/18 (unlisted) hospital 8/20/21 family care bmp, lyne disease 8/25 bmp
- Aktuelle Erkrankungen
- fatigue
- Vorgeschichte
- psoriasis., hypersomnia, osteoarthritis
- Andere Medikamente
- gabapentin. xanax. prilosec,seroquel
- Allergien
- cows milk and dust mites
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 25.08.2021
- Impfdatum
- 18.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Hemiparesis
Peroneal nerve palsy
Pyrexia
Seizure
Tremor
Symptomtext
Starting just after 11:00pm on the 18th of August 2021 I started to slightly shake like the chills. I was not cold or have a fever at this time. While this continued for around an hour or so it gradually became worse until around 1:00am on the 19th of August I started having full body convulsions shaking violently. The left side of my face and body felt like I had no control over it . My face felt like it was drooping and my leg was dragging all on my left side. Eventually around 3:00am the convulsions stopped. While the convulsions finally stopped my fever shot up to 101.9 at this time. I took two Tylenol for the fever and around 4:00 am it finally broke but I was freezing after my temperature went back down to 98.0. The next day I went to my doctor, Dr. I have been extremely weak since these events which have made it difficult to perform my job.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Benazepril/Amlodipine Atorvastatin Meloxicam
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 21.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Hyperhidrosis
Loss of consciousness
Symptomtext
Passed out but immediately came back to. Extreme sweating no fever. Pain in chest, quickly became better after 10 minutes and given water.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Amnesia
Gait disturbance
Loss of consciousness
Symptomtext
Staff reported patient entered facility on 08/11/2021 at approximately 0700, dragging right leg. At approximately 7:15am patient passed out for approximately 1 minute, She became alert within 1 minute but could not remember what happened. EMS was call, patient transferred to ER for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 23.08.2021
- Impfdatum
- 12.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cardiac stress test
Catheterisation cardiac
Chest discomfort
Chest pain
Chills
Electrocardiogram normal
Left ventricular end-diastolic pressure
Myocarditis
Pyrexia
Symptomtext
Received vaccine 8/12 on 8/16 contacted PCP stated had fever , chills and temp at home 101 now having chest pain. Instructed to call 911..patietn refused and wife took to ED In Ed described chest pain as pressure and heaviness in center of chest VS Temp 36.1, pulse 102, BP 144/96 Patient admitted to hospital and discharged 8/19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 4,0
- Labordaten
- EKG normal Stress test BSA 2.29 8/17 Cardiac Cath no obstructive CAD , normal LVEPP, likely myocarditis 2nd to COVID vaccine
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN Asthma Migraines Hypertriglyceridemia Sinus Arrhythmia
- Andere Medikamente
- MVI Albuterol Amitriptyline 10 mg TRICO 145 mg UBRELVY 50 mg Valsartan 80 mg COLCRYS 0,6 mg
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Malaise
Seizure
Syncope
Symptomtext
Patient came in 8/20/21 to get her first dose of Moderna vaccine. Consent form was verified and screening questions were asked. Patient was waiting the required 15 minutes post vaccination and within 5-7 minutes of the post vaccination wait time, patient stated that she was feeling light headed and was going to faint. The pharmacy staff alerted store management and called for medical attention. After stating that she wasn't feeling well, the patient laid down on the floor and fainted for few seconds (5-10 seconds), brief convulsions observed. The patient was alert within a few seconds, able to talk to the pharmacist/ answer questions. The patient called family members while waiting for medical attention to arrive. The patient was continuously being fanned, given an ice-pack and water. The emergency services arrived within 10 minutes as well as the family members. EMS checked patient's vitals and all vitals were within range. The patient went with emergency services to get a complete check up at the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 17.08.2021
- Impfdatum
- 15.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Chest pain
Condition aggravated
Dizziness
Fatigue
Feeling abnormal
Injection site pain
Lymphadenopathy
Pain
Spirometry abnormal
Syncope
Vaccination complication
Symptomtext
I got the vaccine at 3:20pm on Sunday 8/15/21. Woke up with body aches at 1 am Monday 8/16/21. Went downstairs for water and medicine at 2 am. Felt off, went back upstairs, laid in bed, woke up my husband in time to tell him I was going to pass out and then immediately fainted while laying on my bed. I came too, ate bread, took ibuprofen, and went back to sleep. 8/16/21 I experienced normal fatigue, injection site soreness, lymph nodes swollen under injection site arm, body aches. I took ibuprofen every 4-6 hours. Tuesday 8/17/21 around 9 am I started experiencing shortness of breath and mild chest pain. At 10 am I noticed redness and swelling at injection site. I contacted my primary care physician who wanted me to go the the ER. I called my Allergist who was able to see me at 2pm. At 11am I took my albuterol inhaler which improved the symptoms. The appointment with the allergist proved that the albuterol did improve my air way function after a spirometry test. Dr concluded it was asthma exacerbation as a reaction to the COVID-19 vaccine received on 8/15/21. She prescribed albuterol inhaler 3-4x a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- spirometry test at allergist. lung function showed 91%
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma, syncope
- Andere Medikamente
- Advair Diskus, Paxil, Albuterol, Zrytec, Magnesium, Prenatal Supplements
- Allergien
- Sulfa drugs, oxycontin, clindamycin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 17.08.2021
- Impfdatum
- 15.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Additional Details: 7 minutes after receiving 1st dose of Moderna covid vaccine 0.5ml in the left deltoid muscle via IM route, patient felt light head and fainted. He stated this has only happened after giving blood. He regained consciousness immediately, BP check- given orange juice, paramedics were called and on site they evaluated patient and took over care. Upon review, the patient was able to leave and did not need to go to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 16.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaphylactic reaction
Symptomtext
Pt called on 08/13/2021 to cancel the @nd dose. Said she had an anaphylactic reaction and "just got out of the hospital". Pt did not give any details and did not respond to 3 attempts to contact by phone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- 1,0
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Not Known
- Vorgeschichte
- Tobacco Smoker
- Andere Medikamente
- Not known: Patient would not answer phone calls to get more information
- Allergien
- Penicillin and Sulfa
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 15.08.2021
- Impfdatum
- 15.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Fall
Hyperhidrosis
Loss of consciousness
Vomiting
Symptomtext
Patient was okay during vaccine, started getting sweaty a min after the vaccine and threw up for a few min. She then passed out and fell on the floor. She felt okay after passing out. After few second pt regains conscience. Checked her vitals and all was good. EMS was called and everything checked out okay. Pt refused to to be taken to the hospital as she started to feel better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 13.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Seizure
Symptomtext
Patient started having a seizure and fell out of his chair 10 mins after getting the vaccination. The pharmacist called 911 and attended to him. Got him back in the chair and then the patient had a second seizure. The paramedics came and checked him out and said he did not need to go to the hospital if he didn't want to and the patient declined.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Paramedics checked his blood pressure, heart rate, and pulse ox. All where within normal limits.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Feeling hot
Loss of consciousness
Symptomtext
Pt was hot and clammy within 5 minutes of vaccination. She was seated with husband and momentarily passed out for about 30 seconds. She came to and was back to her normal self in about 5 minutes we called emergency services and they came and checked her out and she left feeling fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 10.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dehydration
Fall
Syncope
Symptomtext
Pt fainted and fell after receiving his first covid vaccination. Pt was observed for 30 mins after before being released to go home. Water was provided to pt and he felt fine afterwards. Pt stated he must been dehydrated after a long day of work and felt fine after having some water and rest. Pt was followed up the next day (8/10/21), he was doing fine and very appreciative with the follow up check.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- N/a
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 10.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Loss of consciousness
Symptomtext
Patient passed out about 10 min after shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 09.08.2021
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Syncope
Vision blurred
Symptomtext
Patient came to pharmacy on 08/09 at 09:15 to receive her 1st dose of covid vaccine. After the vaccine administration, patient started complaining of blurred vision and dizziness. Few min later, patient collapsed. Pharmacist was able to get her safely to the floor and in few min, she regained her consciousness. Staff made 911 call.Her legs got elevated to increase blood flow since her BP was reading at 103/74. About 5 min later, the paramedic team arrived and her care was taken over. Her vitals and BG looked normal. She was able to sit up after few min . However, she complained of having HA and syncope, the EMT team transferred her to hospital. Her family was informed about the incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Patient's party was contacted at 02:00pm on 08/09 and was told that she's still at the hospital. The medical care team thinks that she had an allergic rxn to the vaccine. No other information was provided to pharmacy in terms of any medical records.
- Aktuelle Erkrankungen
- Not that was informed
- Vorgeschichte
- N/A
- Andere Medikamente
- Not that we are told by patient
- Allergien
- not that we are told by patient
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 08.08.2021
- Impfdatum
- 08.08.2021
- Beginn
- 08.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
patient fainted in chair. proceeded to lay him on the ground and elevate legs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 03.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Muscle twitching
Seizure
Syncope
Symptomtext
Patient fainted, assisting patient to the floor, he seized or twitched
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Hypotension
Paraesthesia
Seizure
Symptomtext
Patient started feeling "pins and needles". She then had a seizure. Her blood pressure was low and she was extremely hot. The seizure was short. We had her lay on a mat and put ice packs on her and gave her water. She said she hadn't eaten today so we gave her orange juice to raise her blood glucose. Patient is not diabetic. Patient recovered quickly. She refused offer of ambulance. Her boyfriend arrived and said he was going to feed her then take her home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- blood pressure 100/64 8/2/2021 5:00pm
- Aktuelle Erkrankungen
- no known illnesses
- Vorgeschichte
- none
- Andere Medikamente
- Suboxone and sertraline
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 02.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Vomiting
Symptomtext
Patient had a episode of syncope and vomiting. Had to call 911, but patient refused to go to hospital. Patient said he has passed out in the past when gives blood.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- He has cerebral palsy
- Vorgeschichte
- Cerebral palsy
- Andere Medikamente
- PROZAC 40MG -1 CAPSULE DAILY LORAZEPAM 0.5MG -2 TABS ONCE A DAY
- Allergien
- NONE LISTED
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 31.07.2021
- Impfdatum
- 31.07.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Syncope
Symptomtext
Pt got a covid vaccine. got light headed/fainted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NONE, PT WAS GETTING A MODENA VACCINE. PT GOT LIGHT HEADED AND FAINTED
- Vorgeschichte
- NONE, PT WAS GETTING A MODENA VACCINE. PT GOT LIGHT HEADED AND FAINTED
- Andere Medikamente
- NONE, PT WAS GETTING A MODENA VACCINE. PT GOT LIGHT HEADED AND FAINTED
- Allergien
- NONE, PT WAS GETTING A MODENA VACCINE. PT GOT LIGHT HEADED AND FAINTED
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 29.01.2021
- Beginn
- 04.02.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Tinnitus
Symptomtext
Ringing in ears stated with first shot and has progressively gotten a lot worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Skin rashes Face rashes
- Vorgeschichte
- Aortic valve replacement High Blood Pressure High Cholesterol Thyroid disorder (low) Obesity Sleep Apnea
- Andere Medikamente
- Pantoprazole 40 mg Metoprolol Tartrate 50 mg (2 times a day) Benicar 40 mg Levothyroxine 0.112 mg Atorvastatin Calcium 40 mg Xyzal 5mg Triamterene 37.5 mg / HCTZ 25 mg (2 times a week) Nasonex Nasal Spray Aspirin 325 mg Mens Once a Day Mult
- Allergien
- Penicillin Azithromycin Doxycycline Levofloxacin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 24.03.2023
- Impfdatum
- 14.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Heart rate increased
Palpitations
Symptomtext
Three days after being administered the shot, I started having heart palpitations or a feeling of my heart fluttering. These palpitations would last for about 1-2 minutes and would occur 1-3 times per day. The palpitations continued for about 10-12 days and then disappeared. Now 1 year and 7 months later, heart palpitations have returned. This time instead of fluttering, it's a hard fast beating that I feel in my throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Seasonal allergies to ragweed.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 02.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Paraesthesia
Shoulder injury related to vaccine administration
Bursitis
Limb immobilisation
Pain in extremity
Product administered at inappropriate site
Tendonitis
X-ray limb abnormal
Symptomtext
Intense pain in vaccine arm started evening of vaccine injection. I'm daughter,retired RN,& her granddaughter PT, cared for her with ice,Tramadol, topical NSAID, sling,which gave her minimal relief. Intense pain for days. sought treatment at urgent care on 9/5/2021, orthopedic urgent care. Diagnosed with vaccine injury: bursitis/tendonitis of rotator cuff from vaccine injected too high, into bursal sac. Small lady,weight 115.Told to continue same treatment,had to wait a week minimum after vaccine to get steroid injection, appoint.made with Dr. for folowup. Saw him on Sep. 15. He agreed with diagnosis, did xray, and gave her steroid injection. This did offer her some relief.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- xray left shoulder 9/15/2021
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- osteo arthritis, atrial fibrillation
- Andere Medikamente
- amlodipine synthroid,Eliquis,Pepcid, Systane eye drops, tramad
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 23.10.2022
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Dizziness
Heart rate increased
Symptomtext
I had severe chest pain like almost as if someone was both sitting on my chest and stabbing me at the same time. My heart rate wouldn?t come down at all from 100. Which is very unusual for me because my normal rate is usually around 57-60 because I run a lot and I?m very active. I felt very light headed for the majority of the day. This is was all very alarming for me due to the fact that I had previous had to have an echo, and ultrasound, and a chest X-ray, as well as a heart monitor due to a potential heart related incident that occurred a couple years prior. I was fortunate enough after my 2nd dose to have my boyfriend mother, who?s a RN monitor me over night but I did wake up the next day with residual chest pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 01.08.2021
- Beginn
- 01.07.2022
- Tage bis Beginn
- 334,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Palpitations
Supraventricular tachycardia
Symptomtext
Heart palpitations leading to diagnosis of SVT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Between 7/30/2022 to current many dates
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 17.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Therapeutic response unexpected
Symptomtext
This spontaneous case was reported by a patient and describes the occurrence of PARAESTHESIA (Started getting tingling below my knees, started around my knee caps, then makes it's way down to my ankles and toes, sometimes goes away but comes back) and THERAPEUTIC RESPONSE UNEXPECTED (I had a lot of energy after my 2 shots, I was cleaning my house like crazy) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 048F21A and 939902) for COVID-19 vaccination. No Medical History information was reported. On 17-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milligram. On 14-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .5 milligram. On an unknown date, the patient experienced PARAESTHESIA (Started getting tingling below my knees, started around my knee caps, then makes it's way down to my ankles and toes, sometimes goes away but comes back) and THERAPEUTIC RESPONSE UNEXPECTED (I had a lot of energy after my 2 shots, I was cleaning my house like crazy). At the time of the report, PARAESTHESIA (Started getting tingling below my knees, started around my knee caps, then makes it's way down to my ankles and toes, sometimes goes away but comes back) had not resolved and THERAPEUTIC RESPONSE UNEXPECTED (I had a lot of energy after my 2 shots, I was cleaning my house like crazy) outcome was unknown. The patient had no allergies to medications, food and other products. The patient had no acute and chronic illnesses at the time of vaccination. The patient had never been tested or diagnosed with COVID +. No other vaccines were given within 1 month prior to Moderna COVID-19 vaccine. The patient did not had any concomitant medications for any condition. It was reported that about one to two months after receiving the 2nd dose, patient started experiencing tingling just below her knees. The tingling sensation started in her knee caps, and traveled down to her legs, ankles, and toes. Three days later, the tinging went away but it came right back. Patient said that this sensation comes and goes and had never completely gone away since it first started. Patient had been experiencing this in both her legs. At first patient thought it could be neuropathy related, but after reading online she did not thought it was neuropathy as it did not felt like it. Patient believed more in herbal remedies than medications. Additionally, patient stated that she had a lot of energy for 2-3 days after receiving each dose and she got a lot of house cleaning done at that time. No treatment medications were reported. This case was linked to MOD-2022-647616 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 07.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Asthma
Blood test
Computerised tomogram
Condition aggravated
Dyspnoea
Fatigue
Feeling abnormal
Fibromyalgia
Hypoaesthesia
Laboratory test
Magnetic resonance imaging
Pain
Paraesthesia
Pneumonia
Respiratory disorder
X-ray
Symptomtext
I stared getting respiratory issues that turned into pneumonia and from that I have developed severe asthma and constant shortness of breath. I tire easily and can?t even talk for long periods of time. My fibromyalgia pain is much worse and my brain fog is also much worse. I have more numbness and tingling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Multiple CT,s X-rays, blood work, mris, asthma test in hospital that required being in a tube , 3-4 times in ER Docs and tests all began in September 2021.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Fibromyalgia, POTS, depression/anxiety, osteoarthritis, degenerative disk disease, migraines, seasonal allergies, bursitis, arthritis
- Andere Medikamente
- Tramadol, Benadryl, flexeril, Lexapro, daily vitamin, vitamin d, biotin, Valium as needed,
- Allergien
- Shellfish, bee sting, latex, medical tape
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 22.02.2021
- Beginn
- 10.07.2022
- Tage bis Beginn
- 503,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
COVID-19 pneumonia
SARS-CoV-2 test positive
Symptomtext
admitted to hospital for COVID pneumonia, tested covid positive on 7/10/22. started on remdesivir and steroids
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 08.03.2021
- Beginn
- 27.02.2022
- Tage bis Beginn
- 356,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Fatigue
Interchange of vaccine products
SARS-CoV-2 test
Vaccination failure
Tachycardia
Symptomtext
This spontaneous report received from a patient via other manufacturer Pfizer concerned a 45 year old male. Initial information was processed with the additional information received on 10-JUN-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: asthma, hypertension, anxiety, avocado allergy and tree nuts allergy. The patient received Covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805022, expiry: unknown) dose was not reported, 1 total, administered on 08-MAR-2021 at 15:00 in left arm for prophylactic vaccination. Age at time of vaccination 44 years old. The patient additionally received non-company suspect vaccine included: Moderna (Spikevax) vaccine (elasomeran) (dose number in series 2) (form of admin, and route of admin were not reported, batch number: 939902, expiry: unknown) dose was not reported, administered on 25-OCT-2021 at 15:00 in left arm for prophylactic vaccination. Concomitant medications included fluticasone propionate/salmeterol xinafoate (Wixela). On 27-FEB-2022, the patient experienced first Covid symptoms. On 02-MAR-2022, patient tested positive for Covid, thus patient had confirmed Covid-19 infection (dose number in series 2) which led to confirmed clinical vaccination failure (dose number in series 1). Laboratory data included: COVID-19 virus test Positive. The patient received Paxlovid from 02-MAR-2022 to 07-MAR-2022 for Covid-19 treatment. On 08-MAR-2022, patient's symptoms were largely gone except post Covid tachycardia, shortness of breath and fatigue (dose number in series 2). On 10-MAR-2022, Laboratory data included: COVID-19 virus test Negative. On 13-MAR-2022, patient lost sense of smell. Laboratory data included: COVID-19 virus test Positive. The action taken with Covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable. The patient recovered from confirmed Covid-19 infection on 02-APR-2022, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000235175. Sender's Comments: V0: 20220617454- Covid-19 vaccine ad26.cov2.s-confirmed clinical vaccination failure .The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220302; Test Name: COVID-19 VIRUS TEST; Test Result: Positive; Test Date: 20220310; Test Name: COVID-19 VIRUS TEST; Test Result: Negative; Test Date: 20220313; Test Name: COVID-19 VIRUS TEST; Test Result: Positive.
- Aktuelle Erkrankungen
- Allergy to nuts; Anxiety; Asthma; Food allergy; Hypertension
- Vorgeschichte
- -
- Andere Medikamente
- Wixela Inhub
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 08.03.2021
- Beginn
- 27.02.2022
- Tage bis Beginn
- 356,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Fatigue
Interchange of vaccine products
SARS-CoV-2 test
Vaccination failure
Tachycardia
Symptomtext
This spontaneous report received from a patient via other manufacturer Pfizer concerned a 45 year old male. Initial information was processed with the additional information received on 10-JUN-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: asthma, hypertension, anxiety, avocado allergy and tree nuts allergy. The patient received Covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805022, expiry: unknown) dose was not reported, 1 total, administered on 08-MAR-2021 at 15:00 in left arm for prophylactic vaccination. Age at time of vaccination 44 years old. The patient additionally received non-company suspect vaccine included: Moderna (Spikevax) vaccine (elasomeran) (dose number in series 2) (form of admin, and route of admin were not reported, batch number: 939902, expiry: unknown) dose was not reported, administered on 25-OCT-2021 at 15:00 in left arm for prophylactic vaccination. Concomitant medications included fluticasone propionate/salmeterol xinafoate (Wixela). On 27-FEB-2022, the patient experienced first Covid symptoms. On 02-MAR-2022, patient tested positive for Covid, thus patient had confirmed Covid-19 infection (dose number in series 2) which led to confirmed clinical vaccination failure (dose number in series 1). Laboratory data included: COVID-19 virus test Positive. The patient received Paxlovid from 02-MAR-2022 to 07-MAR-2022 for Covid-19 treatment. On 08-MAR-2022, patient's symptoms were largely gone except post Covid tachycardia, shortness of breath and fatigue (dose number in series 2). On 10-MAR-2022, Laboratory data included: COVID-19 virus test Negative. On 13-MAR-2022, patient lost sense of smell. Laboratory data included: COVID-19 virus test Positive. The action taken with Covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable. The patient recovered from confirmed Covid-19 infection on 02-APR-2022, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000235175. Sender's Comments: V0: 20220617454- Covid-19 vaccine ad26.cov2.s-confirmed clinical vaccination failure .The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220302; Test Name: COVID-19 VIRUS TEST; Test Result: Positive; Test Date: 20220310; Test Name: COVID-19 VIRUS TEST; Test Result: Negative; Test Date: 20220313; Test Name: COVID-19 VIRUS TEST; Test Result: Positive.
- Aktuelle Erkrankungen
- Allergy to nuts; Anxiety; Asthma; Food allergy; Hypertension
- Vorgeschichte
- -
- Andere Medikamente
- Wixela Inhub
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 27.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bronchitis
Chest X-ray
Chest pain
Dyspnoea
Pulmonary pain
SARS-CoV-2 test negative
Symptomtext
Woke unable to breathe. Physically i could draw air in and out but I still felt it was never enough. I was woken with this feeling. It passed after 1 hour. Since then I have had chronic pain in my upper chest (bronchial tubes) and was diagnosed at an urgent care with Bronchitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Stethascope check, COVID test rapid at the urgent care (negative), x-ray.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Psoriatic arthritis
- Andere Medikamente
- Acetaminophen 500mg x 6 times per day Tramadol 50mg x 5 times per day Diclofenac 50mg x 2 times per day
- Allergien
- demerol
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 27.10.2021
- Beginn
- 05.03.2022
- Tage bis Beginn
- 129,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
COVID-19
Chills
Fatigue
Influenza
Myalgia
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Tachycardia
Symptomtext
I started off with a sore throat, muscle aches. The 2nd night I had fever and chills like a bad flu. It lasted about 4 days before my fever broke and my body aches went away. I called my doctor and she had me to keep an eye on my pulse oximeter. I was taking nyquil and Benadryl. I did have some stomach issues and tachycardia , that lasted a couple of weeks with some fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- Positive COVID-19
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Metformin, Lisinopril, Rosuvastatin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 06.10.2021
- Beginn
- 08.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood creatine phosphokinase
Electrophoresis protein
Full blood count
Hypoaesthesia
Metabolic function test
Muscular weakness
Paraesthesia
Protein total
Red blood cell sedimentation rate
Vitamin B12
Symptomtext
Symptoms began about 2 days after vaccine administration. She experienced significant weakness, numbness, and tingling to her left arm. It then progressed to her entire body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- basic metabolic CBC protein, total and protein electrophoresis B12 TSH creatine kinase, total sed rate by modified westergren on 11/2
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Vertigo HTN Asthma Chronic sinusitis History of uterine cancer
- Andere Medikamente
- -
- Allergien
- aspirin clindamycin lisinopril losartan mold penicillins shellfish derived sulfa
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 23.08.2021
- Beginn
- 03.03.2022
- Tage bis Beginn
- 192,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Central venous catheterisation
Cholecystectomy
Cough
Device dislocation
Dyspnoea
Enterococcus test positive
Vascular device occlusion
Symptomtext
82-year-old male with a history of CHF, CAD, aortic stenosis status post TAVR presenting to the ED sent in by his nursing home due to a PICC line complication. Patient states that he had a PICC line placed after his cholecystectomy about 2 weeks ago and was in the hospital and per chart review he grew Enterococcus and was placed on antibiotics. Day of admission (3/2/22) the nurse attempted to push the Unasyn when it extravasated and the PICC line became occluded and dislodged. According to patient he has been increasingly SOB and developed cough which is new. Pt was on 2L NC From rehab but does not wear o2 at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 03.03.2022
- Impfdatum
- 08.08.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 14,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropathy
Back disorder
Joint stiffness
Mobility decreased
Symptomtext
She got her vaccine she was pretty much in bed the next day, which she felt was the normal. She is achy and stiff in her joints, and she never had that before. Mainly she has issues with her lower back and knees. Also her hips, shoulder areas and continues to present. She has not sought medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Allergies.
- Andere Medikamente
- Hydroxyzine 25 mg once a day, Cetirizine 10 mg,
- Allergien
- Penicillin.
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 27.08.2021
- Beginn
- 06.09.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase increased
Aspartate aminotransferase increased
Dyspnoea
Fatigue
Pain
Palpitations
Red blood cell sedimentation rate increased
Symptomtext
Generalized body aches, extreme fatigue, heart racing, shortness of breath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 9/15/2021 Sed rate-74 SGOT 38 SGPT-49
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid Arthritis, Hypothyroidism, Osteoporosis, possibly Sjogrens,
- Andere Medikamente
- Orencia, Methotrexate, Prednisone, Folic Acid, Synthroid, Protonix, Atorvastatin, Fosomax, Metoprolol, Magnesium, Calcium supplement, Vitamin D, TheraTears, Estradiol cream, Xiidra eye drops
- Allergien
- Penicillin
- Vorherige Impfungen
- Moderna vaccine 2nd dose-similar symptoms as after 3rd dose
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 06.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Chest pain
Diaphragmalgia
Diarrhoea
Dizziness
Headache
Nausea
Vaccination site erythema
Symptomtext
diarrhea; Chest pain; Diaphragmatic pain; upset stomach; Nausea; red dots around injection site; dizziness; Headache; This spontaneous case was reported by a consumer and describes the occurrence of ABDOMINAL DISCOMFORT (upset stomach), DIZZINESS (dizziness), DIARRHOEA (diarrhea), CHEST PAIN (Chest pain) and DIAPHRAGMALGIA (Diaphragmatic pain) in a 28-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 06-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Aug-2021, the patient experienced HEADACHE (Headache). On an unknown date, the patient experienced ABDOMINAL DISCOMFORT (upset stomach), DIZZINESS (dizziness), DIARRHOEA (diarrhea), CHEST PAIN (Chest pain), DIAPHRAGMALGIA (Diaphragmatic pain), NAUSEA (Nausea) and VACCINATION SITE ERYTHEMA (red dots around injection site). The patient was treated with PARACETAMOL (TYLENOL) ongoing since an unknown date at an unspecified dose and frequency. On 07-Aug-2021, HEADACHE (Headache) had resolved. At the time of the report, ABDOMINAL DISCOMFORT (upset stomach), DIZZINESS (dizziness), DIARRHOEA (diarrhea), CHEST PAIN (Chest pain), DIAPHRAGMALGIA (Diaphragmatic pain), NAUSEA (Nausea) and VACCINATION SITE ERYTHEMA (red dots around injection site) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medication was provided. Took tylenol for symptoms, patient states that only helped with headache but other symptoms do not go away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 20.08.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 147,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Dyspnoea
Fatigue
Oropharyngeal pain
Symptomtext
Initially had sore throat and was really tired with low-grade temperatures. About a week, began to feel short of breath. Had telehealth visit and was recommended to get Covid pill.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Crohn's Disease; Epilepsy
- Andere Medikamente
- Cimzia; Lamictal
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 12.02.2021
- Beginn
- 14.03.2021
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Biopsy skin
Blood test
Cutaneous vasculitis
Dysstasia
Feeling abnormal
Gait disturbance
Impaired quality of life
Limb discomfort
Loss of personal independence in daily activities
Mobility decreased
Pain in extremity
Peripheral swelling
Rash
Rash erythematous
Surgery
Ultrasound scan
X-ray
Symptomtext
I now have Leukocytoclasia vasculitis (LCV) which took me 10 months, 17 doctors, 7 specialists, multiple misdiagnosis, and 2 unnecessary irreversible surgeries to finally diagnose me. My quality of life has been horrible. I can't walk or stand for long periods of time, travel without major issues, I can't do any physical activities including dancing, cleaning around the house or walking quickly up the stairs of my home, cannot wear even 1 inch heels, and have to wear shoes to support my feet due to the extreme level of pain, swelling and discomfort. I am often stuck in bed and having to be carried to the restroom or have a caretaker assist with getting me what I need. I was not even able to visit more than two dress shops yesterday to try on wedding dresses without swelling up and having horrendous bumps and Red rashes all over my legs. I was previously a very active 38 year older who, ran, danced, skated, and was a fashionista that lived for my heels, but my new world is that I can't even get around my 3 story home, can't walk my dog on most days, can't even stand to cook in the kitchen or do normal things. I'm miserable and am bringing this to your attention after speaking to someone at V safe check-in and being disregarded as if it wasn't to do with my vaccine now only to find out it is after eliminating my mild case of Crohns which has been in remission for several years. Time occurrence has built from once a month to always always.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Ultrasounds, x rays, blood work, and skin biopsy.
- Aktuelle Erkrankungen
- Crohn's
- Vorgeschichte
- Crohn's disease, adenomyosis, and now also hidradenitis suppurativa
- Andere Medikamente
- Remicade and Loestrin
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 23.08.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arrhythmia
Cardiac ablation
Inappropriate schedule of product administration
Symptomtext
Systemic: Cardiac Disorder (diagnosed by MD)-Medium, Error: Booster Given Too Early-, Additional Details: Patient stated that she had seen a cardiologist and determined that the patient had developed an arrhythmia due to the vaccination. The patient had to be placed on flecaninide and have an ablation done.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 08.09.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 45,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray
Chest pain
Dysmenorrhoea
Dyspnoea
Electrocardiogram normal
Heavy menstrual bleeding
Oligomenorrhoea
Palpitations
Symptomtext
Experiencing intermittent shortness of breath, heart palpitations, chest pain since receiving the 2nd dose. Experiencing longer, heavier, more painful menstrual cycles since receiving the 2nd dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG - normal Chest Xray - normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Unknown neurological episode in 2014, Meningoencephalitis
- Andere Medikamente
- Lexapro Daily Women's Vitamins Prebiotic/Probiotic
- Allergien
- Allergic to tropical fruit, bananas, kiwis, possible latex allergy
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 05.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 22,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Amnesia
Dysgeusia
Headache
Migraine
Nightmare
Salivary hypersecretion
Speech disorder
Vomiting
Symptomtext
Body producing excessive saliva for the first 2.5 weeks. Than taste of metal. Followed horrific headaches. Been taking excedrine pills but can't take too many. Month of December, I have been experiencing severe memory loss. Co workers whom I worked for years, can't recall their name. Now my speech has been suffering. Can't articulate a conversion. Later this month, keep having random nightmares consecutively. Today is December 19, 2021. Spent the night and morning vomiting with migraine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Breast pain
Injection site pain
Paraesthesia
Sleep disorder
Symptomtext
First two vaccines were Pfizer so you know with no problems. Left arm in shot location pain and slight soreness in left axillary by midnight. Woke up several times with axilla pain gradually worsening. Tylenol and ice packs that next day. Pain in axilla worsened thru the next day extending into left breast; continued ice packs and Tylenol and reported to doctor office which just referred me to vaccine pharmacy who referred to cdc who referred me to file this. 11/25/2021 pain decreased to tolerable with only Tylenol. 11/26/2021 left axilla only tender when pressure applied. Around 4pm started having tingling in both hands which gradually extended up both arms then tingling over whole body when standing, so now I'm just sitting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cardiac Arrhythmias, obesity, factor v, Hypothyroid, gastroparesis, hiatal hernia, umbilical hernia, fibromyalgia, anxiety, Osteoporosis, Osteoarthritis, bone spurs, left rotator cuff problems, bursitis in hips
- Vorgeschichte
- Same as item 11.
- Andere Medikamente
- Pneumonia vaccine, eliquis, Verapamil, lipitor, fenofibrate, Levothyroxine, Amitriptyline, Clonazapam, Tylenol
- Allergien
- Levaquin, Gabapentin
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Arthralgia
Balance disorder
Chest pain
Confusional state
Muscular weakness
Nausea
Neck pain
Swollen tongue
Tremor
Symptomtext
Approximately 20 minutes after vaccination, patient began having tremors in her chin which spread to her legs within 2-3 minutes. She declined epinephrine but did receive an oral dose of liquid diphenhydramine before her husband took her to the hospital. Once there, she was given IV steroids, famotidine, lorazepam, and diphenhydramine to control her reaction. She was discharged the same day with a prescription for a prednisone taper and famotidine. Over the next two days she experienced confusion, continued tremors, leg weakness, nausea, chest pain, stomach pain, neck pain, swollen tongue, poor balance, and pain in joints.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ITP
- Andere Medikamente
- -
- Allergien
- Patient showed the pharmacist an extensive list of confirmed drug allergies, including but not limited to NSAIDs, sulfa antibiotics, multiple other antibiotics, as well as multiple other blood pressure medications. She described the range of reactions she had experienced in the past.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 12.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Electromyogram
Injection site induration
Injection site nodule
Injection site pruritus
Injection site swelling
Loss of personal independence in daily activities
Mobility decreased
Muscular weakness
Peripheral swelling
Pyrexia
X-ray
Symptomtext
Hives, welts, blisters from injection site to middle of arm near elbow. Was told it was localized and could take the 2nd shot. Took 2nd shot 9/9/21 (IM, RA, Lot # 048F21A) On the 10th, couldn't close right hand; right hand didn't work. Fever of 103 degrees lasted 18 hours. Knots on both arm after the injections, Swollen and hard and itched at the injection site. Severe swelling in the right hand. Been to orthopedics, is going to the reumatologist. Is right handed, so having difficulty with basic daily activities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- EMG, X-rays
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure, Borderline diabetes
- Andere Medikamente
- Metoprolol 100 mg 2x daily, Metformin ER 500 mg 3x daily, Atorvastitin 10 mg 1x daily, Chlorthalidone 25mg 1x daily
- Allergien
- Penicillin class, Pentazoine class, Metradone class, Meperidine class, Losartin, Potassium, Lisinopril, Hydrochlorophiazide, Tetanus shot, Codeine, Opiate derivatives, Cephalexin, Bee pollen, Atenolol, Amlodipine Besylate
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chest pain
Condition aggravated
Dizziness
Dyspnoea
Fatigue
General physical health deterioration
Headache
Injection site mass
Injection site pain
Insomnia
Somnolence
Symptomtext
From the 2nd vaccine, I still have a sore spot and a lump where the vaccination was administered, I am having problems breathing, chest pain on the left side, fatigue all of the time, problems sleeping, sleepiness during the day (I thought this was because of my problems with sleeping), pounding headache EVERYDAY since the 1st vaccine, daily joint pain, but mostly in my hips and shoulders, dizziness and issues with medical or physical exertion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Chest x-ray, blood work, EKG, oxygen and others may have been administered at the hospital. I am unsure of the actual date but I believe it was approximately October 13, 2021.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Barrett's Esophagus
- Andere Medikamente
- Protonix, multi-vitamin, flaxseed, fish oil, CoQ10
- Allergien
- Dilaudid
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Cardiac flutter
Chest discomfort
Electrocardiogram normal
Heart rate irregular
Musculoskeletal chest pain
X-ray normal
Symptomtext
later that night chest tightness, tender to the touch, heart fluttering, heart beat off rhythm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- ekg-normal xray-normal bloodtest-normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- blood pressure meds
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dehydration
Dizziness
Dizziness postural
Epistaxis
Eye contusion
Fall
Gait disturbance
Joint injury
Lip injury
Nasal injury
Pain
Paraesthesia
Poor quality sleep
Skin abrasion
Skin laceration
Symptomtext
Received the 2nd dose of Moderna approx 8:45 am on 11/4/21. Started feeling the tingly and achy side effects by about 7 pm that night. Went to bed feeling pretty achy and weak and had a somewhat restless sleep. Just before 5 am, our home fire alarms went off - my husband and I walked through the house to turn them off. On my way back upstairs, I started feeling very weak and dizzy. I stopped at the hall bathroom to use the bathroom. Upon standing up I was feeling incredibly weak and dizzy as if I was about to pass out. I grabbed the sink vanity and the door frame, and the next thing I remember is waking up on the floor with my husband who rushed to my side when he heard the thud of my body hitting the floor. I had a bloody nose, a gash on the bridge of my nose, a gash near my eyebrow, and a slightly split lip (all on my right side of face). Also scraped my elbow. Got back to bed with the help of my husband but felt like I could barely walk I was so weak. Also felt slightly dehydrated. Put a cold compress and ice on my face and rested for the next 6 hours. Will likely have a black eye and suspect I may possibly have broken my nose during my fall. NOTE: I was forced to get this vaccine in order to keep my job; I did not otherwise intend to get the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Leiden Factor VI
- Andere Medikamente
- 81 mg aspirin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Mobility decreased
Pain in extremity
Symptomtext
Soreness in upper left arm for 3-4 days hurt to lift over head.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Migraines
- Andere Medikamente
- Emgality
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Chest pain
Costochondritis
Electrocardiogram normal
Symptomtext
11/01/2021 I began walking to the bus at 7:45am I felt a bad pain in my chest, it lasted thru out the day. I went into my doctor the same day. I have Costo Chondrointis and it is still ongoing to this day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 11/01/2021 I had a blood panel-normal 11/01/2021 EKG-normal
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Multivitamin Marnea IED
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Hypoaesthesia oral
Immediate post-injection reaction
Paraesthesia oral
Sensory loss
Symptomtext
Immediately after all 3 shots had facial numbness. It was sensory loss only; all motor was intact. No other symptoms. After the first shot it lasted about 10 minutes; 2nd shot as bout 25 minutes. Numbness just gradually left. After 3rd shot the numbness was the same but I had lip numbness for 2 hours. They then started tingling similar to anesthetic wearing off after dental work. Then I was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxine, nasocort, vit d3, magnesium, claritin, vit b complex
- Allergien
- PCN, sulfa
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 15.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Biopsy
Condition aggravated
Goitre
Neck pain
Pain in extremity
Tenderness
Thyroid gland scan abnormal
Symptomtext
Following the vaccine I had a lot of pain in my left arm as expected. I had pain in my left shoulder and all along the left side of my neck and the back of my neck. There was tenderness along the left side which I assumed were swollen lymph nodes, which I expected. Eventually intense arm, shoulder and neck pain along the back of my neck subsided. The neck pain has come and gone. I realized what I thought was the swollen lymph node was the goiter enlarging.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I had previous history of a thyroid goiter on my left side that had remained the same size since discovery two years ago in 2019 (TI- RAD 2-3 rating) however on Oct 11, 2021 I had an ultrasound and the goiter had grown 50 percent in size and was rated (TI-RAD 5 by radiologist). The growth triggered a biopsy conducted on Oct 28, 2021 and I'm still waiting the results. I'm only reporting because the area that I thought was just a swollen lymph node after vaccination ended up being the thyroid goiter enlarging.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Previous Deep Vein Thrombosis, Temporal Mandibular Joint Syndrome (TMJ), unexplained belching
- Andere Medikamente
- Vitamin D 2000 IU/day, eliquis 2.5 mg 2x per day, culturelle probiotic
- Allergien
- Allergic to tizanidine and multiple pollen allergies
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 13.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy to vaccine
Aphonia
Blood pressure inadequately controlled
Dental discomfort
Inappropriate schedule of product administration
Loss of personal independence in daily activities
Mobility decreased
Muscle spasms
Pain
Peripheral swelling
Renal haemorrhage
Urticaria
Vaccination site pain
Visual impairment
Symptomtext
More than 35 days for 2nd dose; kidneys were bleeding; there is a sore at injection site; Had hives; feet were swollen; lost voice; started having vision problems in left eye/left eye has been shut for no reason; dental problems that she never had; muscle cramps; severe pain; blood pressure has not been controlled; can't run anymore; Have all these new allergies/Can't eat peanut butter anymore/Can't eat eggs anymore; Cannot work; This spontaneous case was reported by a consumer and describes the occurrence of RENAL HAEMORRHAGE (kidneys were bleeding) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902.) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was reported. Concurrent medical conditions included Egg allergy (Can't eat eggs), Food allergy (Can't eat peanut butter), Penicillin allergy, Drug allergy (Norco) and Drug allergy (cephalosporins). Concomitant products included EPINEPHRINE (EPIPEN) for Allergy. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Aug-2021, the patient experienced RENAL HAEMORRHAGE (kidneys were bleeding) (seriousness criterion medically significant), URTICARIA (Had hives), PERIPHERAL SWELLING (feet were swollen), APHONIA (lost voice), VISUAL IMPAIRMENT (started having vision problems in left eye/left eye has been shut for no reason), DENTAL DISCOMFORT (dental problems that she never had), MUSCLE SPASMS (muscle cramps), PAIN (severe pain), BLOOD PRESSURE INADEQUATELY CONTROLLED (blood pressure has not been controlled) and VACCINATION SITE PAIN (there is a sore at injection site). In August 2021, the patient experienced LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Cannot work), MOBILITY DECREASED (can't run anymore) and ALLERGY TO VACCINE (Have all these new allergies/Can't eat peanut butter anymore/Can't eat eggs anymore). On an unknown date, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (More than 35 days for 2nd dose). On 20-Aug-2021, RENAL HAEMORRHAGE (kidneys were bleeding) had resolved. At the time of the report, LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (Cannot work), URTICARIA (Had hives), PERIPHERAL SWELLING (feet were swollen), APHONIA (lost voice), VISUAL IMPAIRMENT (started having vision problems in left eye/left eye has been shut for no reason), DENTAL DISCOMFORT (dental problems that she never had), MUSCLE SPASMS (muscle cramps), PAIN (severe pain), BLOOD PRESSURE INADEQUATELY CONTROLLED (blood pressure has not been controlled), MOBILITY DECREASED (can't run anymore), VACCINATION SITE PAIN (there is a sore at injection site) and ALLERGY TO VACCINE (Have all these new allergies/Can't eat peanut butter anymore/Can't eat eggs anymore) had not resolved and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (More than 35 days for 2nd dose) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No treatment medication information was mentioned by reporter Patient had not been vaccinated with 2nd dose. It was stated that, she had not treated her or prescribed her any medications. They keep on saying she had antibodies of 2500. She states because of these new allergies she had to carry an EpiPen with her all the time. Company Comment This case concerns a 43-year-old, female patient with no relevant medical history, who experienced the unexpected event of Renal hemorrhage (Kidney bleeding). The event occurred approximately 1 day after the first dose of mRNA-1273 (Moderna Covid-19 vaccine). The rechallenge was not applicable, as the event happened after the first dose. The benefit-risk relationship of mRNA-1273 (Moderna Covid-19 vaccine) is not affected by this report.; Sender's Comments: This case concerns a 43-year-old, female patient with no relevant medical history, who experienced the unexpected event of Renal hemorrhage (Kidney bleeding). The event occurred approximately 1 day after the first dose of mRNA-1273 (Moderna Covid-19 vaccine). The rechallenge was not applicable, as the event happened after the first dose. The benefit-risk relationship of mRNA-1273 (Moderna Covid-19 vaccine) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (Norco); Drug allergy (cephalosporins); Egg allergy (Can't eat eggs); Food allergy (Can't eat peanut butter); Penicillin allergy
- Vorgeschichte
- Comments: No medical history was reported.
- Andere Medikamente
- EPIPEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 23.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dyspnoea
Migraine
Nausea
Vomiting
Symptomtext
Body chills and shortness of breath @2100 on 10/21 Nausea and vomiting @ 2200 on 10/21 100.5 F temperature @ 2300 on 10/21 102.1 F temperature and migraine @ 1700 on 10/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lo loestrin fe Prenatal vitamins SlowFe Minocycline
- Allergien
- Eye dilation medication
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 18.10.2021
- Impfdatum
- 16.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Malaise
Myalgia
Pyrexia
Symptomtext
Severe Myalgia, Fever, and malaise. Shortness of breath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 27.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Arthralgia
Chest discomfort
Chest pain
Chills
Dizziness
Dyspnoea
Fatigue
Headache
Hyperhidrosis
Hypoaesthesia
Inflammation
Influenza like illness
Lethargy
Limb discomfort
Muscular weakness
Myalgia
Palpitations
Symptomtext
she woke up with sweats; muscles were weak; arms felt heavy/ Arms felt like led; pressure on the chest continued intermittently/ chest feels a lot of pressure; pain in chest continued intermittently/ chest pain has become less but still come and go; she gets out of breathe; Headache feels like ice pick and stabbed her cranium through the brain/headache lasts for 10 minutes or 5-10second; tired and was mostly in bed; headache; fever; body chills; joint pain; muscle pain; numbness in the arm is now faded/ still has that sensation in the left arm; Tingling/ Left side of face has tingling sensation which she still has now; Stomach pain; inflammation on both side of her body/her body is very inflamed; tiredness; she woke up with weird tingling/ weird sensation in both her arms; pressure on her chest/ /chest feels a lot of pressure; pain in her chest; she developed flu like symptoms; lethargy; heart palpitation/ heart stuff still continuing; immediately she got dizzy in the room/lots of dizziness that continued for the rest of the day; heart began to race/ heart beating fast/ heart beating hard/ heart felt as if it will pop out/ been over a week and a half and has not stopped; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (immediately she got dizzy in the room/lots of dizziness that continued for the rest of the day), PALPITATIONS (heart began to race/ heart beating fast/ heart beating hard/ heart felt as if it will pop out/ been over a week and a half and has not stopped), CHEST DISCOMFORT (pressure on her chest/chest feels a lot of pressure), CHEST PAIN (pain in her chest) and INFLUENZA LIKE ILLNESS (she developed flu like symptoms) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 27-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Sep-2021, the patient experienced DIZZINESS (immediately she got dizzy in the room/lots of dizziness that continued for the rest of the day) and PALPITATIONS (heart began to race/ heart beating fast/ heart beating hard/ heart felt as if it will pop out/ been over a week and a half and has not stopped). On 03-Oct-2021, the patient experienced CHEST DISCOMFORT (pressure on her chest/ /chest feels a lot of pressure), CHEST PAIN (pain in her chest), INFLUENZA LIKE ILLNESS (she developed flu like symptoms), LETHARGY (lethargy), PALPITATIONS (heart palpitation/ heart stuff still continuing), PARAESTHESIA (she woke up with weird tingling/ weird sensation in both her arms), HYPOAESTHESIA (numbness in the arm is now faded/ still has that sensation in the left arm), PARAESTHESIA (Tingling/ Left side of face has tingling sensation which she still has now), ABDOMINAL PAIN UPPER (Stomach pain), INFLAMMATION (inflammation on both side of her body/her body is very inflamed), FATIGUE (tiredness), HEADACHE (headache), PYREXIA (fever), CHILLS (body chills), ARTHRALGIA (joint pain) and MYALGIA (muscle pain). On 04-Oct-2021, the patient experienced HYPERHIDROSIS (she woke up with sweats), MUSCULAR WEAKNESS (muscles were weak), LIMB DISCOMFORT (arms felt heavy/ Arms felt like led), CHEST DISCOMFORT (pressure on the chest continued intermittently/ chest feels a lot of pressure), CHEST PAIN (pain in chest continued intermittently/ chest pain has become less but still come and go), DYSPNOEA (she gets out of breathe), HEADACHE (Headache feels like ice pick and stabbed her cranium through the brain/headache lasts for 10 minutes or 5-10second) and FATIGUE (tired and was mostly in bed). The patient was treated with NAPROXEN at a dose of 400 mg. On 04-Oct-2021, HYPERHIDROSIS (she woke up with sweats), MUSCULAR WEAKNESS (muscles were weak) and FATIGUE (tired and was mostly in bed) had resolved. At the time of the report, DIZZINESS (immediately she got dizzy in the room/lots of dizziness that continued for the rest of the day), LETHARGY (lethargy), HYPOAESTHESIA (numbness in the arm is now faded/ still has that sensation in the left arm), FATIGUE (tiredness), HEADACHE (headache), PYREXIA (fever), CHILLS (body chills), ARTHRALGIA (joint pain) and MYALGIA (muscle pain) had resolved, PALPITATIONS (heart began to race/ heart beating fast/ heart beating hard/ heart felt as if it will pop out/ been over a week and a half and has not stopped), PALPITATIONS (heart palpitation/ heart stuff still continuing), CHEST DISCOMFORT (pressure on the chest continued intermittently/ chest feels a lot of pressure), CHEST PAIN (pain in chest continued intermittently/ chest pain has become less but still come and go), PARAESTHESIA (Tingling/ Left side of face has tingling sensation which she still has now) and HEADACHE (Headache feels like ice pick and stabbed her cranium through the brain/headache lasts for 10 minutes or 5-10second) had not resolved and CHEST DISCOMFORT (pressure on her chest/ /chest feels a lot of pressure), CHEST PAIN (pain in her chest), INFLUENZA LIKE ILLNESS (she developed flu like symptoms), PARAESTHESIA (she woke up with weird tingling/ weird sensation in both her arms), LIMB DISCOMFORT (arms felt heavy/ Arms felt like led), DYSPNOEA (she gets out of breathe), ABDOMINAL PAIN UPPER (Stomach pain) and INFLAMMATION (inflammation on both side of her body/her body is very inflamed) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient reported that her weight was 140. Patient reported that she will not be getting her second dose. Patient reported that fever, body chills, joint pain, muscle pain, lethargy, tiredness, headache lasted for 2.5 days. Patient consulted NP and was prescribed with steroids medication which she has not taken yet. Patient discloses that she had COVID twice before and did not have antibodies when she went to check for them (Before receiving her first shot) No concomitant medications were reported. On 3 Oct 2021,Chest X-ray and Electrocardiogram was normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 23.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Condition aggravated
Dyspnoea
Heart rate
Ventricular extrasystoles
Symptomtext
symptoms and frequency increased/she woke up with worse symptoms; PVC (Premature Ventricular Contractions); shortness of breath; weakness; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (shortness of breath), ASTHENIA (weakness), VENTRICULAR EXTRASYSTOLES (PVC (Premature Ventricular Contractions)) and CONDITION AGGRAVATED (symptoms and frequency increased/she woke up with worse symptoms) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 23-Aug-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Aug-2021, the patient experienced DYSPNOEA (shortness of breath) (seriousness criterion hospitalization) and ASTHENIA (weakness) (seriousness criterion hospitalization). In September 2021, the patient experienced VENTRICULAR EXTRASYSTOLES (PVC (Premature Ventricular Contractions)) (seriousness criterion hospitalization). On 27-Sep-2021, the patient experienced CONDITION AGGRAVATED (symptoms and frequency increased/she woke up with worse symptoms) (seriousness criterion hospitalization). The patient was hospitalized for 1 day due to ASTHENIA, CONDITION AGGRAVATED, DYSPNOEA and VENTRICULAR EXTRASYSTOLES. At the time of the report, DYSPNOEA (shortness of breath), ASTHENIA (weakness), VENTRICULAR EXTRASYSTOLES (PVC (Premature Ventricular Contractions)) and CONDITION AGGRAVATED (symptoms and frequency increased/she woke up with worse symptoms) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Aug-2021, Heart rate: irregular (Inconclusive) irregular. On 02-Sep-2021 was her first emergency room visit. She went to the emergency room where they admitted her and kept her overnight. They sent her home the next day with beta blockers. Patient's husband was not sure about her concomitant medications either besides Pepcid. This case concerns a 68-year-old female patient with no relevant medical history, who experienced the unexpected serious events of Dyspnoea, Asthenia, and Ventricular extrasystoles. The events occurred approximately 6 days after receiving the third dose of Moderna COVID-19 Vaccine. The re-challenge was not applicable as the events occurred following the third dose of vaccine. The benefit-risk relationship of Moderna COVID-19 Vaccine is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 27-Sep-2021: Follow up received contain patient demographic include date of birth, age, weight, new event added , concomitant medication , drug information include batch number, case upgrade to serious .; Sender's Comments: This case concerns a 68-year-old female patient with no relevant medical history, who experienced the unexpected serious events of Dyspnoea, Asthenia, and Ventricular extrasystoles. The events occurred approximately 6 days after receiving the third dose of Moderna COVID-19 Vaccine. The re-challenge was not applicable as the events occurred following the third dose of vaccine. The benefit-risk relationship of Moderna COVID-19 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 20210828; Test Name: heartbeat; Test Result: Inconclusive; Result Unstructured Data: irregular.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 23.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Migraine
Symptomtext
Headaches and migraines daily since shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Citalopram 40mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 01.09.2021
- Beginn
- 05.09.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Diplopia
Symptomtext
September 5, 2021, horizontal double vision upon awakening lasting 20 minutes. September 10, 2021, horizontal double visio upon awakening lasting 40 minutes. I experinceed similar episodes following the first and second doses of the vaccine and submitted a VAERS for both today. I was seen by my Primary Care Physician, an opthalmologist and a neuro-opthalmologist following the second episodes. A cause for the double vision was not determined but the clinicians said it was not related to the vaccine. Since the double vision occurred following the third dose I felt reporting it was warranted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic lymphocytic leukemia Mitral valve prolapse Palpitations
- Andere Medikamente
- Multivitamin ASA 81 mg Zyrtec 10 mg Metoprolol Succinate ER 25 mg Vitamin C 500 mg Calcium citrate +D 630mg Zinc 50 mg Glucosamine/chondroitin Fish Oil 1,200 mg
- Allergien
- Macrodantin
- Vorherige Impfungen
- Double vision after first and second dose of the Moderna vaccine, 02/15/2021 and 03/15/2021.
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Feeling jittery
Flushing
Heart rate
Heart rate increased
Hypoaesthesia
Hypoaesthesia oral
Symptomtext
Numb Tongue/Tip of the tongue still numb; Jittery; Numb Face with tingling; Flushing; Chest pain; Heart was fast; Shortness of breath/Hard time breathing; This spontaneous case was reported by a consumer and describes the occurrence of HYPOAESTHESIA ORAL (Numb Tongue/Tip of the tongue still numb), FEELING JITTERY (Jittery), HYPOAESTHESIA (Numb Face with tingling), FLUSHING (Flushing) and CHEST PAIN (Chest pain) in a 36-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 16-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Aug-2021, the patient experienced HYPOAESTHESIA ORAL (Numb Tongue/Tip of the tongue still numb), FEELING JITTERY (Jittery), HYPOAESTHESIA (Numb Face with tingling), FLUSHING (Flushing), CHEST PAIN (Chest pain), HEART RATE INCREASED (Heart was fast) and DYSPNOEA (Shortness of breath/Hard time breathing). At the time of the report, HYPOAESTHESIA ORAL (Numb Tongue/Tip of the tongue still numb), FEELING JITTERY (Jittery), HYPOAESTHESIA (Numb Face with tingling), FLUSHING (Flushing), CHEST PAIN (Chest pain), HEART RATE INCREASED (Heart was fast) and DYSPNOEA (Shortness of breath/Hard time breathing) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 16-Aug-2021, Heart rate: fast fast. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. After the shot the patient waited more than 15 minutes and within 30 minutes felt a numb tongue, jittery, numb face with tingling, flushing, chest pain, her heart was fast, shortness of breath/hard time breathing for about 6 hours. But the tip of tongue was still numb since then. No Concomitant medications were provided. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210816; Test Name: Heart rate; Result Unstructured Data: fast
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 01.10.2021
- Impfdatum
- 25.03.2021
- Beginn
- 09.04.2021
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Dyspnoea
Fatigue
SARS-CoV-2 test positive
Symptomtext
Patient presented to ED on 4/9/21 with weakness, fatigue, and SOB. Found to be covid positive after fully vaccinated. Patient was treated for covid 19 pneumonia during admission
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 12,0
- Labordaten
- covid positive test on 4/9. Chest x ray on 4/9 representing covid 19 pneumonia
- Aktuelle Erkrankungen
- Not applicable
- Vorgeschichte
- Polymorphic leukemia of the T cell type, Hypertension, Chronic kidney disease, atrial flutter
- Andere Medikamente
- Zyrtec, esoperazole, temazepam
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 30.09.2021
- Impfdatum
- 06.09.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Angiogram abnormal
Anticoagulant therapy
Cardioversion
Chest pain
Coronary artery occlusion
Electrocardiogram abnormal
Resuscitation
Thrombectomy
Ventricular tachycardia
Symptomtext
Moderna COVID-19 Vaccine EUA: Inpatient hospitalization or prolongation of existing hospitalization (ST Elevation MI) Patient received Moderna Vaccines on 8/9/2021 and 9/6/2021. Presented to ED after waking with severe chest pain. Initial EKG showed possible ST elevation MI. he was given aspirin. While in transit to ED and while in ED, he went into ventricular tachycardia required cardioversion as well as CPR. In the ED, he required additional cardioversion due to VT. Patient underwent intervention to the RCA with thrombectomy and intracoronary tPA. However, blood flow was not reestablished and patient was brought back to the cath lab the next day. An angiogram showed total occluded RCA with some collaterals from left to right. He did have an angiogram in July of 2021 that showed moderate disease in the RCA with positive remodeling. Showed no significant stenosis in the RCA. He had COVID-19 vaccination 3 days before that. The concern was that his MI may be due to hypercoagulable state, therefore, he will be on Eliquis and Plavix, but not aspirin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- H/O A-FIb, Bladder Cancer, CKD, CAD, Enlarged Prostate, Gout, History of Prior Ablation, Hyperlipidemia, hypothyroid, Pneumonia due to COVID-19 in July 2020, Sleep apnea, History of stroke, Thoracic aortic aneurysm, Lumbar radiculopathy.
- Andere Medikamente
- Amitriptyline 10 mg QD, Aspirin 81 mg QD, Azelastine Nasal, rosuvastatin 5 mg MWF, Isosorbide Mononitrate 15 mg QD, Levothyroxine 75 mcg QD, Tizanidine 4 mg QD.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 31.08.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
Chest discomfort
Decreased appetite
Drainage
Dysphagia
Dyspnoea
Fatigue
Feeling of body temperature change
Flushing
Heart rate increased
Hyperhidrosis
Limb discomfort
Lymphadenopathy
Nasal congestion
Pain
Swelling face
Symptomtext
Severe abdominal stabbing pain from 8PM to 8:30PM same day 8/31/2021; lasted 30 minutes. extreme pain made me cry. 8am - 12PM on 9/1/2021 - flushing of face, some facial swelling. 9am - 12PM on 9/1/2021 - nasal conjection, swollen glands, difficulty swallowing, feeling of allergies; rapid heart beat. Feeling heavy in the legs; tired body. 12pm -6PM on 9/1/2021 - nasal drainage, less allergic response. Body aches, heavy in legs, sweaty palms and feet, rapid and fluttering heart beat, feeling of cot and hold, chills, temp 99. 6PM on 9/1/2021 - 9/3/2021 - no appetite, tired. Since 9/1/2021 - I have had some days of rapid heartbeat, shortness of breath and tight chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies only
- Andere Medikamente
- MultiVitamin, Vitamin C
- Allergien
- Soaps, fragrences, cats, dust, mold, pollen, trees, grass, dog
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 13.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chest pain
Fear
Hypoaesthesia
Neuralgia
Paraesthesia
X-ray
Symptomtext
3 days after received the Moderna vaccine I started to get sharp pains on the left side in my chest, it kept coming and going. I didn't think too much of it and thought it could be from gas possibly. As the days went on I kept feeling this pain and then it started to feel like I had gas trapped in the chest. By Monday, September 20, 2021 the chest pains would not go away and it started to worry me. My mid week of that week I called a Cardiologist to schedule and appointment and it was scheduled for two weeks out. By Friday, September 24, 2021 I was still having the sharp chest pains that would not go away, I'm a healthy 34 year old and have no underlying health issues and a high immunity. After the sharp chest pains on the morning of Friday, September 24 around 9:00 am I started to have pain go towards my inner shoulder and then tingling and numbness down my left arm, my fingers began to go numb and tingling. I began to worry and thought I may be having a heart attack. I decided to go the ER & Urgent Care to have it checked out by doing an Xray of my chest. The doctor saw to heart inflammation and didn't say what it could be, but ever since then I constantly have random chest pains with nerve pain going down my left arm. I've never had this in my life, until after I received the 1st dose of the Moderna vaccine - 3 days after the vaccine. I am afraid to get my 2nd dose of the Moderna since my reaction can be even worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Xray taken only - 9/24/21
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None
- Andere Medikamente
- multi-vitamin, Vitamin D, fish oil
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 15.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal loss of weight
Asthenia
Balance disorder
Chills
Dizziness postural
Dyspnoea exertional
Fall
Feeling hot
Gait disturbance
Head discomfort
Headache
Hypoaesthesia
Symptomtext
Patient's significant other brought him into the hospital because of severe headache and right-sided numbness. Patient had been feeling numb from the right mid forearm distally and from the lower third of the right leg distally since yesterday at 4:30pm. The numbness is described as constant, with no relieving factors, no exacerbating factors. He has waning and waxing episodes. He had difficulty walking because of losing balance today. He has had headache for 2 days, the headache is constant, better with the sumatriptan, exacerbated with loud noises, non-progressive, 10 out of 10 pain level when he came to the ED. Pressure and throbbing-like in nature and localized on the right side of the head. Patient's significant other states that yesterday at approx 5:30pm, she heard a thud sound in the kitchen and found patient lying on the floor responsive. Patient says they opened the refrigerator and then next thing they knew, they woke up lying on the floor. He has been having exertional dyspnea since yesterday. He has been feeling more warm than usual for 1 week but did not check his temperature at home. He has been having chills and shivers from time to time over the past week. He feels dizzy while standing up. He has generalized weakness. He lost 8 lbs unintentionally in the past month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- hyperlipidemia
- Andere Medikamente
- atorvastatin, cetirizine, vitamin D, pregabalin, sumatriptan, tramadol, Co-Q-10
- Allergien
- duloxetine, metoprolol, verapamil
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 24.09.2021
- Impfdatum
- 18.08.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling cold
Gait disturbance
Hypoaesthesia
Paraesthesia
Peripheral coldness
Skin discolouration
Symptomtext
Hands are still cold and numb,feet have remained ice cold,[feet] feel a little cold; Really hurts to walk; Pins and needles; she was really cold; Feet and hands went numb; They were a little blue and purplish hasn't gotten better,[hands] turning a little blue; This spontaneous case was reported by a consumer and describes the occurrence of FEELING COLD (she was really cold), HYPOAESTHESIA (Feet and hands went numb), SKIN DISCOLOURATION (They were a little blue and purplish hasn't gotten better,[hands] turning a little blue), PERIPHERAL COLDNESS (Hands are still cold and numb,feet have remained ice cold,[feet] feel a little cold) and GAIT DISTURBANCE (Really hurts to walk) in a 23-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 0481217 and 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 18-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Sep-2021 at 6:30 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 15-Sep-2021, the patient experienced FEELING COLD (she was really cold), HYPOAESTHESIA (Feet and hands went numb) and SKIN DISCOLOURATION (They were a little blue and purplish hasn't gotten better,[hands] turning a little blue). On 16-Sep-2021, the patient experienced PERIPHERAL COLDNESS (Hands are still cold and numb,feet have remained ice cold,[feet] feel a little cold) and PARAESTHESIA (Pins and needles). 16-Sep-2021, the patient experienced GAIT DISTURBANCE (Really hurts to walk). At the time of the report, FEELING COLD (she was really cold), HYPOAESTHESIA (Feet and hands went numb), SKIN DISCOLOURATION (They were a little blue and purplish hasn't gotten better,[hands] turning a little blue), PERIPHERAL COLDNESS (Hands are still cold and numb,feet have remained ice cold,[feet] feel a little cold), GAIT DISTURBANCE (Really hurts to walk) and PARAESTHESIA (Pins and needles) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 14.09.2021
- Beginn
- 14.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Chest discomfort
Chest pain
Dysphagia
Dyspnoea
Eye swelling
Fatigue
Flushing
Headache
Hyperhidrosis
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Insomnia
Lethargy
Mouth swelling
Rash
Symptomtext
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Severe, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Systemic: Tachycardia-Mild, Systemic: Unable to Sleep-Medium, Systemic: Weakness-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Dyspnoea
Symptomtext
Severe chest pain and shortness of breath lasting two-three days. Symptoms resolved spontaneously, no treatment received
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High cholesterol
- Andere Medikamente
- Rapatha injections Nexletol
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 05.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Arthralgia
Intermenstrual bleeding
Migraine
Pain
Symptomtext
menstrual spotting that lasted for 4 days; migraine that lasted for 3 days; extreme body/joint aches that lasted for 2 days; stomach pain that lasted for 8 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- high blood pressure, poly cystic ovarian syndrome
- Andere Medikamente
- doxazosin, progesterone, armour thyroid, nadalol, amlodipine besylate
- Allergien
- n/a
- Vorherige Impfungen
- lump size of a tennis ball on arm, weakness in arm - both lasted for months
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 10.08.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
Chest pain
Chills
Heart rate
Hypotension
Malaise
Myalgia
Nausea
Symptomtext
My blood pressure was 101/52/ low blood pressure; CHEST PAIN; NAUSEA; CHILLS; MYALGIA; I received the dose at 4pm, I wasn't feeling well when I went to bed.; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (I received the dose at 4pm, I wasn't feeling well when I went to bed.), HYPOTENSION (My blood pressure was 101/52/ low blood pressure), CHEST PAIN (CHEST PAIN), NAUSEA (NAUSEA) and CHILLS (CHILLS) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 020F21A and 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Medical history was not provided by the reporter. Concomitant products included MOMETASONE FUROATE (FLONASE [MOMETASONE FUROATE]) and MULTIVITAMIN [VITAMINS NOS] for an unknown indication. On 10-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Sep-2021 at 4:00 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Sep-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced MALAISE (I received the dose at 4pm, I wasn't feeling well when I went to bed.). On 09-Sep-2021, the patient experienced HYPOTENSION (My blood pressure was 101/52/ low blood pressure), CHEST PAIN (CHEST PAIN), NAUSEA (NAUSEA), CHILLS (CHILLS) and MYALGIA (MYALGIA). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) for Adverse event, at an unspecified dose and frequency. At the time of the report, MALAISE (I received the dose at 4pm, I wasn't feeling well when I went to bed.), HYPOTENSION (My blood pressure was 101/52/ low blood pressure), CHEST PAIN (CHEST PAIN), NAUSEA (NAUSEA), CHILLS (CHILLS) and MYALGIA (MYALGIA) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 09-Sep-2021, Blood pressure measurement: 101/52 (Low) LOW. On 09-Sep-2021, Heart rate: 116 (High) HIGH.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210909; Test Name: BLOOD PRESSURE; Result Unstructured Data: LOW; Test Date: 20210909; Test Name: HEART RATE; Result Unstructured Data: HIGH
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- FLONASE [MOMETASONE FUROATE]; MULTIVITAMIN [VITAMINS NOS]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 20.09.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Feeling cold
Throat tightness
Symptomtext
Patient received Moderna second dose 9/20/21 at 0852. At 0903 staff was notified by patient that her throat feels like it's closing up and that it feels cold to swallow. Patient instructed not to eat or drink at this time. She states she?s allergic to several foods and drugs but didn't want to specify, however she?s not allergic to any ingredient in the vaccine that she knows of, she also normally carries an epi pen but the one she has has expired so she left it at home. Patient stated that she didn't eat anything all day, she took her epilepsy medication and drank coffee. Vitals obtained at 0904. Patient gave verbal consent to assess and treat. Patient at this point stated she feels as if she can?t breath, states she feels as if her throat is closing up. epipen 1/1000 IM administered to the left lateral thigh by staff at 0905. 911 was called by clinical site lead. Patient was reassessed in 5 minutes, second set of vitals taken at 0909 BP 122/62 P100 SPO2 99%. Patient states the epipen isn't working and she feels the same, however vitals remain stable and patient remained awake alert and oriented x4. Continued to monitor vitals taken at 0918 BP 124/70 P97 SPO2 97%. While keeping patient calm and awaiting rescue. Rescue arrived at 0923, rescue started IV line with NS. Patient was Transported to ER rescue. Rescue incident report #1218856.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- patient was transported to ER for further follow up
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- PATIENT STATED SHE TOOK HER EPILEPSY MEDICATION THIS MORNING BUT UNBALE TO VERIFY NAME OF MEDICATION
- Allergien
- PATIENT STATED THAT SHE IS ALLERGIC TO EVERYTHING, WHEN ASK TO SPECIFY SHE DIDN'T
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 18.09.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Dizziness
Limb mass
Pain
Palpitations
Peripheral swelling
Pyrexia
Rash erythematous
Symptomtext
Dizziness and heart palpitations upon receiving injection. Red rash, bruising, sore & swollen arm. Fever and masses knot in arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- WPW, CHF, Asthma, Diabetes Type II
- Andere Medikamente
- None
- Allergien
- Vicadine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 15.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Dizziness
Dysphagia
Dyspnoea
Fatigue
Headache
Hypoaesthesia
Injection site pain
Lethargy
Pain
Paraesthesia
Pruritus
Tachycardia
Throat tightness
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Headache-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Tachycardia-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Systemic: Weakness-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 11.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Chest pain
Dyspnoea
Neck pain
Pruritus
Rash
Rash macular
Symptomtext
Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Chest Tightness / Heaviness / Pain-Severe, Additional Details: Pt states that she has blotches all over her body, experiencing neck pain and chest felt heavy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 14.09.2021
- Impfdatum
- 07.09.2021
- Beginn
- 07.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Arthralgia
Chills
Consciousness fluctuating
Fall
Fatigue
Joint injury
Mobility decreased
Pain
Pain in extremity
Pyrexia
X-ray
Symptomtext
I experienced all the common side effects: sore arm, fatigue, fever, chills, body aches within the first 12 hours of receiving my second dose of the Moderna shot. I passed in and out of consciousness 4 times during the early hours of Wednesday morning, September 8th resulting in a fall in my bathroom onto the tile floor. I have severely injured my left knee. I cannot bend my knee and have constant pain in it. I have had a x-ray and will have a MRI to see if the meniscus or MCL is torn. If my husband hadn?t caught me I passed out when he did I would have further injured myself and likely hit my head.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- X-ray of left knee on Thursday, September 9th, 2021 MRI scheduled for Thursday, September 16th, 2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Rosuvastatin 10mg/ 3x week CoQ10
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 12.09.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Echocardiogram
Electrocardiogram normal
Laboratory test abnormal
Wheezing
Symptomtext
Chest pain, wheezing. Irregular labs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Ekg heart echo
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Pineapples
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 10.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Menstruation delayed
Nausea
Paraesthesia
Pyrexia
Symptomtext
Patient had 2 days of fever and nausea starting on 8/14/21. Tingling and numbness in the right arm and is continuous and current since 8/14/21. No menses for 1 month since 1st vaccine. No signs of pregnancy - pt has had her menses regularly prior to vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- nothing
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- U
- Eingang
- 08.09.2021
- Impfdatum
- 24.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dyspnoea
Fatigue
Feeling of body temperature change
Headache
Myalgia
Symptomtext
I feel short of breath; feel tired; headaches; body ache; I've been hot and cold; Dry cough; This spontaneous case was reported by a consumer and describes the occurrence of FEELING OF BODY TEMPERATURE CHANGE (I've been hot and cold), COUGH (Dry cough), DYSPNOEA (I feel short of breath), MYALGIA (body ache) and FATIGUE (feel tired) in a 44-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Anxiety, Depression, Migraine and Sleep disorder. On 24-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-Aug-2021, the patient experienced FEELING OF BODY TEMPERATURE CHANGE (I've been hot and cold), COUGH (Dry cough), MYALGIA (body ache) and HEADACHE (headaches). On 26-Aug-2021, the patient experienced DYSPNOEA (I feel short of breath) and FATIGUE (feel tired). At the time of the report, FEELING OF BODY TEMPERATURE CHANGE (I've been hot and cold), COUGH (Dry cough), DYSPNOEA (I feel short of breath), MYALGIA (body ache), FATIGUE (feel tired) and HEADACHE (headaches) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment medication was reported by patient. Patient reported concomitant medication for anxiety, depression, migraines and sleep. Patient reported no history of COVID-19 infection nor history of myocarditis and pericarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety; Depression; Migraine; Sleep disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Flushing
Hypoaesthesia
Hypoaesthesia oral
Palpitations
Paraesthesia
Symptomtext
Within thirty mins of having vaccine tongue started to go numb after about 1 hour after the vaccine face started to get tingling/numbness fast heart palpitaions felt like chest was getting pushed on then felt flusing of blood to my head this lasted for about 4-5 hours after vaccine administered. To date I still have numbness on the tip of my tongue that has not went away. I never had this numbness prior to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Anxiety,Migraines,neck & back spasms
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 06.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chest pain
Symptomtext
Patient reports "chest pain" that started the morning of 9/8/21 as well as, pain in the lower back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Bisoprolol/HCTZ 5/6.25 mg
- Allergien
- Penicillins
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 14.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Dysstasia
Hypoaesthesia
Insomnia
Loss of personal independence in daily activities
Malaise
Mobility decreased
Neck pain
Pain
Pain in extremity
Symptomtext
not doing well at all; fingers are numb; can't sleep; can't do anything; can barely move the shoulder; can barely stand because of the pain in the back; Pain is spreading across her back and into her left shoulder and arm; Pain is spreading across her back and into her left shoulder and arm; She can barely move shoulder; The pain travelled from the right arm/shoulder, across the back, to the top of the left shoulder and also to the neck.; it became beyond the pain she knows, this is totally different/It gets everyday more severe; woke up with severe arm pain, entire upper arm\ the pain is spreading across her back and into her left shoulder and arm; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (woke up with severe arm pain, entire upper arm\ the pain is spreading across her back and into her left shoulder and arm), MALAISE (not doing well at all), HYPOAESTHESIA (fingers are numb), INSOMNIA (can't sleep) and LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (can't do anything) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Complex regional pain syndrome (since 17 year). On 14-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Aug-2021, the patient experienced PAIN IN EXTREMITY (woke up with severe arm pain, entire upper arm\ the pain is spreading across her back and into her left shoulder and arm). On 17-Aug-2021, the patient experienced PAIN (it became beyond the pain she knows, this is totally different/It gets everyday more severe). On an unknown date, the patient experienced MALAISE (not doing well at all), HYPOAESTHESIA (fingers are numb), INSOMNIA (can't sleep), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (can't do anything), MOBILITY DECREASED (can barely move the shoulder), DYSSTASIA (can barely stand because of the pain in the back), BACK PAIN (Pain is spreading across her back and into her left shoulder and arm), ARTHRALGIA (Pain is spreading across her back and into her left shoulder and arm), MOBILITY DECREASED (She can barely move shoulder) and NECK PAIN (The pain travelled from the right arm/shoulder, across the back, to the top of the left shoulder and also to the neck.). The patient was treated with NAPROXEN SODIUM (ALEVE) at a dose of 6 a day. At the time of the report, PAIN IN EXTREMITY (woke up with severe arm pain, entire upper arm\ the pain is spreading across her back and into her left shoulder and arm), MALAISE (not doing well at all), HYPOAESTHESIA (fingers are numb), INSOMNIA (can't sleep), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (can't do anything), MOBILITY DECREASED (can barely move the shoulder), DYSSTASIA (can barely stand because of the pain in the back), BACK PAIN (Pain is spreading across her back and into her left shoulder and arm), ARTHRALGIA (Pain is spreading across her back and into her left shoulder and arm), MOBILITY DECREASED (She can barely move shoulder), NECK PAIN (The pain travelled from the right arm/shoulder, across the back, to the top of the left shoulder and also to the neck.) and PAIN (it became beyond the pain she knows, this is totally different/It gets everyday more severe) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Complex regional pain syndrome (since 17 year)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 05.09.2021
- Impfdatum
- 04.09.2021
- Beginn
- 05.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Migraine
Symptomtext
Severe migraine NOT relieved by migraine medication. My migraines are controlled and will dissipate with medication-this headache would not respond to medication
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- Levothyroxine, Amerge, multi vitamin, calcium carbonate
- Allergien
- Aspirin and morphine
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 10.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Heart rate
Myalgia
Symptomtext
Myalgia; chest pain; shortness of breath; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (Myalgia), CHEST PAIN (chest pain) and DYSPNOEA (shortness of breath) in a 22-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 10-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-Aug-2021, the patient experienced MYALGIA (Myalgia), CHEST PAIN (chest pain) and DYSPNOEA (shortness of breath). At the time of the report, MYALGIA (Myalgia), CHEST PAIN (chest pain) and DYSPNOEA (shortness of breath) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 13-Aug-2021, Heart rate: increased (High) increased. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product was not provided by the reporter. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210813; Test Name: Heart rate; Result Unstructured Data: increased
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 14.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Blood glucose
Chills
Constipation
Fatigue
Feeling abnormal
Headache
Infection
Pain
Palpitations
Stress
White blood cell count
Symptomtext
Slight infection; I was constipated; This morning I was kneeling over because of stomach pain; Pain was horrible; I was tired; Chills; Headache that would come and go in waves on Sunday; Brain fog; Stress induced because she was anxious in receiving the vaccine; I could feel my heart palpitating that night; This spontaneous case was reported by a consumer and describes the occurrence of PALPITATIONS (I could feel my heart palpitating that night), INFECTION (Slight infection), CONSTIPATION (I was constipated), ABDOMINAL PAIN UPPER (This morning I was kneeling over because of stomach pain) and FEELING ABNORMAL (Brain fog) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for an unreported indication: GLUTATHIONE and Vitamin C. Concomitant products included LISINOPRIL for an unknown indication. On 14-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 14-Aug-2021, the patient experienced PALPITATIONS (I could feel my heart palpitating that night) and STRESS (Stress induced because she was anxious in receiving the vaccine). On 15-Aug-2021, the patient experienced FEELING ABNORMAL (Brain fog), FATIGUE (I was tired), CHILLS (Chills) and HEADACHE (Headache that would come and go in waves on Sunday). On 16-Aug-2021, the patient experienced INFECTION (Slight infection), CONSTIPATION (I was constipated), ABDOMINAL PAIN UPPER (This morning I was kneeling over because of stomach pain) and PAIN (Pain was horrible). On 15-Aug-2021, CHILLS (Chills) had resolved. On 16-Aug-2021, ABDOMINAL PAIN UPPER (This morning I was kneeling over because of stomach pain), FEELING ABNORMAL (Brain fog) and HEADACHE (Headache that would come and go in waves on Sunday) had resolved. At the time of the report, PALPITATIONS (I could feel my heart palpitating that night), INFECTION (Slight infection), STRESS (Stress induced because she was anxious in receiving the vaccine), PAIN (Pain was horrible) and FATIGUE (I was tired) outcome was unknown and CONSTIPATION (I was constipated) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 16-Aug-2021, Blood glucose: high (High) WBC count as well as glucose was high. On 16-Aug-2021, White blood cell count: high (High) WBC count as well as glucose was high. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment medication included was Antibiotics for the increased WBC count.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210816; Test Name: Glucose; Result Unstructured Data: WBC count as well as glucose was high; Test Date: 20210816; Test Name: WBC count; Result Unstructured Data: WBC count as well as glucose was high
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 31.08.2021
- Impfdatum
- 27.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Chest pain
Cough
Fatigue
Headache
Heart rate increased
Rash
Urticaria
Wheezing
Symptomtext
hives aross arms and body within 24 hours headache fatigue chest pain rapid heart beat pain in left side of abdoamin wheezing/cough 32-48 hours after injection went to urgent care facility on the monday after reciving my shot on friday
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- general physician looked at me listened to my breathing inspected remannits of rash prescribed azithromycin 250mg 6 tablets methyiprednisolone 4mg 21 tablets triamcinolone acetonide cream
- Aktuelle Erkrankungen
- strep
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- not any known
- Vorherige Impfungen
- hives at injection site of my first shot
- Staat
- OH
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 31.08.2021
- Impfdatum
- 15.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Aphasia
Blood test
Computerised tomogram
Dysarthria
Echocardiogram
Electrocardiogram
Extra dose administered
Hemiparaesthesia
Magnetic resonance imaging
Memory impairment
Migraine
Paraesthesia
Scan with contrast
Transient ischaemic attack
Symptomtext
6 days after receiving the booster shot for Covid (Moderna), on 8/21/2021 I was admitted to the hospital for 3 days for TIA/possible complex migraine. The entire right side of my body leg to head and to the middle of my trunk/face was numb, tingling, and I did hot have good control of my limbs. Additionally, I could not form sentences, speech was very slurred, and I could not remember things when asked on the spot. I had recurrence of these same symptions one week later on 8/28/21, but did not result in an admission to the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hemiparaesthesia
- Hospital-Tage
- 3,0
- Labordaten
- I had CT, CT with contrast, EKG, bloodwork, MRI, MRI with contrast, and Echocardiogram testing done while in the hospital on 8/21/21 through 8/23/23. These tests did not show signs of significant stroke, but I was discharged with a diagnosis of TIA. I had bloodwork and stroke protocol testing done in the ER on 8/28/21. I was discharged with a diagnosis of complex migraine. I have now been referred to a neurologist for follow up and to determine if what I've experienced is TIA related or migraine related. I have never had any episode like this ever before in my life.
- Aktuelle Erkrankungen
- ear infection in left ear
- Vorgeschichte
- none
- Andere Medikamente
- lisinoprol/HTZ 10/12.5, claritin OTC, Ibuprofen as needed
- Allergien
- Wellbutrin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 31.08.2021
- Impfdatum
- 04.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Arthralgia
Back pain
Constipation
Dysphonia
Gait disturbance
Headache
Hypoaesthesia
Influenza
Nausea
Pain
Pain in extremity
Paraesthesia
Pruritus
Vision blurred
Symptomtext
stomach problems; symptoms of the flu; eyes were blurry; difficulty walking; back hurt; hoarse; tingling in her hands; aches all over/pains all over; numbness in her face; legs hurt/feet hurt; itching all over; constipated; nausea/nauseous; headache; sharp pains in her wrist; This spontaneous case was reported by a consumer and describes the occurrence of ABDOMINAL DISCOMFORT (stomach problems), INFLUENZA (symptoms of the flu), VISION BLURRED (eyes were blurry), GAIT DISTURBANCE (difficulty walking) and BACK PAIN (back hurt) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 (she threw out her back and was taken to the hospital and tested positive for COVID-19.) on 02-Jun-2021, Brain tumor operation, Endoscopy gastrointestinal (3 polyps removed from endoscopy of gastrointestinal tract 3 years ago), Cataract operation in January 2021, Cataract operation in February 2021 and Tooth extraction (her teeth removed and got dentures which continue to irritate her gums.). Concurrent medical conditions included Blood pressure high. Concomitant products included OLMESARTAN from 04-Aug-2021 to an unknown date for Blood pressure high, TIZANIDINE for Muscle relaxant, HYDROCHLOROTHIAZIDE (HYDRODIURIL), FAMOTIDINE, DICYCLOMINE [DICYCLOVERINE], CURCUMA LONGA (TURMERIC [CURCUMA LONGA]), CARBIDOPA, CALCIUM, MAGNESIUM, ZINC, MOMETASONE FUROATE (FLONASE [MOMETASONE FUROATE]), ESTRADIOL and GLYCERYL TRINITRATE (NITROGLYCERIN) for an unknown indication. On 04-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Aug-2021, the patient experienced ABDOMINAL DISCOMFORT (stomach problems), INFLUENZA (symptoms of the flu), VISION BLURRED (eyes were blurry), GAIT DISTURBANCE (difficulty walking), BACK PAIN (back hurt), DYSPHONIA (hoarse), PARAESTHESIA (tingling in her hands), PAIN (aches all over/pains all over), HYPOAESTHESIA (numbness in her face), PAIN IN EXTREMITY (legs hurt/feet hurt), PRURITUS (itching all over), CONSTIPATION (constipated), NAUSEA (nausea/nauseous), HEADACHE (headache) and ARTHRALGIA (sharp pains in her wrist). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency and MACROGOL 3350 (MIRALAX) for Constipation, at an unspecified dose and frequency. On 08-Aug-2021, PRURITUS (itching all over) had resolved. At the time of the report, ABDOMINAL DISCOMFORT (stomach problems), INFLUENZA (symptoms of the flu), VISION BLURRED (eyes were blurry), GAIT DISTURBANCE (difficulty walking), BACK PAIN (back hurt), DYSPHONIA (hoarse), PARAESTHESIA (tingling in her hands), PAIN (aches all over/pains all over), HYPOAESTHESIA (numbness in her face), PAIN IN EXTREMITY (legs hurt/feet hurt), NAUSEA (nausea/nauseous), HEADACHE (headache) and ARTHRALGIA (sharp pains in her wrist) outcome was unknown and CONSTIPATION (constipated) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. Concomitant medication reported eropenol for restless sleep 5 mg, aropadol and women's vitamin. Patient stated she was nauseous the day before reporting and drank buttermilk. Patient had an appointment with her doctor next week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure high
- Vorgeschichte
- Medical History/Concurrent Conditions: Brain tumor operation; Cataract operation; COVID-19 (she threw out her back and was taken to the hospital and tested positive for COVID-19.); Endoscopy gastrointestinal (3 polyps removed from endoscopy of gastrointestinal tract 3 years ago); Tooth extraction (her teeth removed and got dentures which continue to irritate her gums.)
- Andere Medikamente
- HYDRODIURIL; FAMOTIDINE; DICYCLOMINE [DICYCLOVERINE]; TURMERIC [CURCUMA LONGA]; CARBIDOPA; CALCIUM; MAGNESIUM; ZINC; FLONASE [MOMETASONE FUROATE]; ESTRADIOL; NITROGLYCERIN; TIZANIDINE; OLMESARTAN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 25.08.2021
- Beginn
- 26.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Migraine
Nausea
Pain
Sensitive skin
Symptomtext
Starting 8/26 at 03:00AM, patient began experiencing extreme skin sensitivity over entire body. Described that "wearing a shirt felt like knives." Extreme fatigue and pain as expected post-vaccine, along with migraine headache. Pain all over body that patient described as "feeling like my entire body is bruised" with no physical presentation of bruising. Persistent nausea lasting multiple days, refractory to home remedies, responsive only to meclizine. Nausea is now manageable but still disruptive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis, psoriasis, ADHD, depression, anxiety, agoraphobia, degenerative disc disease in lumbar region, immune suppression from Cosentyx therapy for psoriasis
- Andere Medikamente
- Meloxicam 15mg QD, Propranolol 10mg QD PRN, Buspirone 15mg BID, Duloxetine 40mg BID, Trazodone 50mg QHS, Chlorzoxazone 500mg BID, Amphetamine salts 10mg QAM, Cosentyx 300mcg SQ Q4 weeks, Vitamin D3 50mcg QD, Cetirizine 10mg QD, HydroEye sup
- Allergien
- Bupropion
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dyspnoea
Symptomtext
it's getting slightly worse/more noticeable than it was on Saturday; having a lot of shortness of breath/I have not taken a satisfying breath of air since Saturday/I have to take a deep breath to take a good breath of air; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (having a lot of shortness of breath/I have not taken a satisfying breath of air since Saturday/I have to take a deep breath to take a good breath of air) and CONDITION AGGRAVATED (it's getting slightly worse/more noticeable than it was on Saturday) in a 23-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 06-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 07-Aug-2021, the patient experienced DYSPNOEA (having a lot of shortness of breath/I have not taken a satisfying breath of air since Saturday/I have to take a deep breath to take a good breath of air). On 11-Aug-2021, the patient experienced CONDITION AGGRAVATED (it's getting slightly worse/more noticeable than it was on Saturday). At the time of the report, DYSPNOEA (having a lot of shortness of breath/I have not taken a satisfying breath of air since Saturday/I have to take a deep breath to take a good breath of air) and CONDITION AGGRAVATED (it's getting slightly worse/more noticeable than it was on Saturday) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient stated that even her yawns are not satisfying. Concomitant product information was not reported. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 27.08.2021
- Impfdatum
- 31.07.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray normal
Chest pain
Cough
Diarrhoea
Epistaxis
Lethargy
Night sweats
Pyrexia
Rhinorrhoea
Symptomtext
fever less than 100 degrees, cough, runny nose, lethargy, diarrhea, night sweats, blood in mucous, chest pain . patient went to emergency room on 08/24/2021. was evaluated, but no treatment was given. still having some of these symptoms intermittently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- chest xray negative.
- Aktuelle Erkrankungen
- pharyngitis sinusitis
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- lisinopril
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 14.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Cold type haemolytic anaemia
Cough
Cyanosis
Dyspnoea
Extra dose administered
Headache
Influenza like illness
Pain
Pain in extremity
Peripheral coldness
Rhinorrhoea
Sneezing
Symptomtext
Sore arm and aches for 2 days, then flu like symptoms, sneezing, coughing, running nose, breathing issues, headaches and body aches, Then yesterday, my left pinky finger turned blue and cold. It appears to be cold agglutinin disease which i did not have until the 3rd vaccination. The first 2 vaccinations only resulted in sore arm for 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None since the vaccination
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Polycemia vera, Multiple Myeoloma, spinal cord damage, possible MS
- Andere Medikamente
- Clonazapam, Oxycodone, Tamsulosin, aspirin, ibuprofen, magnesium, milk thistle, flax oil, fish oil, vitamin-d, gamma e complex, alpha lipoic acid, dihydromyricetin, choline & Inositol Ginkgo Biloba
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 18.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Pain
Palpitations
Symptomtext
Events: 14 hours of heart palpations, body aches, chills, headache for 5 days. I did not seek treatment for the heart palpations since they were in the overnight hours. I decided to seek help if it reached the noon hour of the next day and they resolved by 10:00am on the 8-19. The daily headaches were resolved by daily Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Progesterone, E2/E3/test HRT (Estrogen)
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 23.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest discomfort
Chest pain
Fatigue
Insomnia
Lethargy
Pain
Tachycardia
Symptomtext
Systemic: Body Aches Generalized-Medium, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Joint Pain-Severe, Systemic: Tachycardia-Severe, Systemic: Unable to Sleep-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 08.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Pain in extremity
Symptomtext
Sore left arm, tightness in chest, sharp chest pains.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Depression, hypothyroid, TBI
- Andere Medikamente
- Levothyroxine, bupropion, armour, fluoxetine, birth control, fish oil, vitamin c, vitamin D
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Dizziness
Fatigue
Injection site pruritus
Injection site rash
Lymphadenopathy
Muscle spasms
Nausea
Pain in extremity
Tremor
Vaginal haemorrhage
Symptomtext
Day 1 - nausea, felt like insides were shaking, lightheaded, sore arm, insides were cramping, Day 2 - tired, felt like inside were shaking, Day 3-tired, nausea, cramping , Day 5-stomach cramping, Day 6-vaginal bleeding (lasting 8 days), Day 7- developed arm soreness again, swollen lymph nodes under arm on side of injection, Day 8-continue arm sore, developed rash, itching, on arm side of injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 18.08.2021
- Impfdatum
- -
- Beginn
- 07.08.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- UN / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Dyspnoea
Dyspnoea exertional
Fatigue
Feeling abnormal
Headache
Malaise
Pyrexia
Symptomtext
I did not have a reaction after the first dose. After taking the second dose (08/07/2021) 12 hours later I got very sick, I had a fever, headache, joint pain and shortness of breath. On 08/10/2021 I improved a bit, days have passed and I am still very tired and out of breath if I do any physical exertion. I do not feel normal, this worries me, it's been more than 10 days and I do not feel well. What should I do?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- I don't have any.
- Aktuelle Erkrankungen
- Ninguno
- Vorgeschichte
- Ninguno
- Andere Medikamente
- Ninguno
- Allergien
- Ninguno
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 18.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Chest discomfort
Chest pain
Fatigue
Feeling abnormal
Headache
Injection site pain
Insomnia
Lethargy
Malaise
Pain
Symptomtext
Around three hours post-vaccination, I developed a headache and arm pain at the injection site. As the afternoon progressed, the headache intensified and I became more tired and lethargic, and just not feeling well. Around 9 PM I laid down to try and go to sleep but the severe pain in my arm made it difficult. The pain radiated down to my elbow, up into my armpit, and across my chest. I experienced some chest tightness. The headache remained. All of my joints ached and were painful. I took an epsom salt bath and soaked. I took Tylenol and Bendryl to try and help me sleep. The next day, I feel drained, weak, lethargic, and tired. I still have a headache and don't feel well. It has been over 24 hours since my injection and I still don't feel like myself.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Wheat/Gluten due to Celiac Disease, Hashimotos Thyroiditis
- Andere Medikamente
- Synthroid 0.075mg, Paroxetine 10mg, Tylenol, Bendaryl (Diphenhydramine)
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 18.08.2021
- Impfdatum
- 18.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Fall
Musculoskeletal stiffness
Speech disorder
Symptomtext
PATIENT FELL PRIOR TO COMING INTO STORE OUT OF CAR AND GOT A BLOODY ELBOW. INSIDE PATIENT HAD RECEIVED VACCINE AND WAITED HIS 15 MINUTES. HE WAS ASKED IF HE WAS DOING OK AND HE SAID IM FINE. HE WAS TALKING AND RESPONIVE WHILE IN THE STORE. HIS CARE GIVER SAID HE WAS FINE. FROM THE TIME HE LEFT THE STORE HIS CAREGIVER SAID SHE NEEDED HELP TO GET HIM IN HIS CAR HE FELL FROM HIS WHEELCHAIR AGAIN AND HE WAS STIFF AND NOT TALKING. PATIENT WAS TAKEN TO medical facility
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- BLINDNESS AND WHEELCHAIR BOUND
- Andere Medikamente
- NOT KNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 14.08.2021
- Impfdatum
- 14.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paraesthesia oral
Symptomtext
Patient was advised to stay at observation area for 30 minutes after the first dose of COVID19 shot. Previously she had anaphylactic reaction to oral medication that required Epi-pen. She was knowledgeable regarding the allergy reaction and what she was allergic to. She was released by her doctor to get the shot even though she was on isatuximab and carfizomib. About 15 minutes after the injection, her tongue felt funny. I gave her 10ml of diphenhydramine 12.5mg/5ml orally. She was advised to stay for another 20 minutes. She felt ok after the medicine so I released her back home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- cancer
- Vorgeschichte
- -
- Andere Medikamente
- 10ml Diphenhydramine 12.5mg/5ml orally 15 minutes after Moderna was given
- Allergien
- omeprazole, codeine, allopurinol, valium
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 13.08.2021
- Impfdatum
- 01.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Palpitations
Rash
Symptomtext
Starting on 08/03/2021 (day three) rash down both arms and on chest. Heart palpitations with some chest pain lasting about three days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Took benadryl for rash which helped. Heart palpitations got less and less as well as chest pain as time went on. Did not go to doctor or hospital.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal Asthma
- Andere Medikamente
- None
- Allergien
- Penicilin, Cefouroxime, Amooxicillin, Ampicillin, Sulfamethoxazole and Trimethoprim
- Vorherige Impfungen
- Rash on arms and chest.
- Staat
- AZ
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 12.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Hypertension
Nausea
Vomiting
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Headache-Severe, Systemic: Hypertension-Severe, Systemic: Nausea-Severe, Systemic: Vomiting-Severe, Additional Details: blood pressure 144/81. no history of high blood pressure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Choking
Dyspnoea
Eye movement disorder
Feeling hot
Incoherent
Unresponsive to stimuli
Symptomtext
Per patient's request Moderna Covid19 vaccine first dose administered by APhA IMZ certified Pharmacy Technician. After receiving the shot and while being observed for 15 minutes in waiting area, patient started to complain of being hot and gradually slouch over chair. I rushed to support up patient then his head involuntarily rocked back abruptly and his eyes rolled back. Technician told to dial 911 emergency. Patient gradually moved to the floor on his back with legs raised. Blood pressure taken (201/97). While on floor patient started to choke and struggle to breathe so 1 dose of Epipen Autoinjector 0.3mg administer into left thigh at 1:45pm. Patient then was placed in recovery position with breathing improving. Blood pressure check again at 1:55pm at 193/75. Patient was not completely responsive or coherent. Store's defibrillator retrieved while continued to monitor patient's pulse and airways until paramedics arrived. Paramedics apply EKG patches and sat patient up then decided to transported patient to hospital for continue observation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Blood pressure 201/97 After laying on floor with epipen given 193/75
- Aktuelle Erkrankungen
- Type 2 DM
- Vorgeschichte
- Type 2 DM
- Andere Medikamente
- METFORMIN 500MG TAB ATORVASTATIN 40MG TAB VITAMIN D3(CHOLE) 5,000 IU CAP LISINOPRIL 40MG TAB FINASTERIDE 5MG TAB AMLODIPINE 2.5MG TAB FARXIGA 10MG TAB GLIPIZIDE 10MG TAB
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Dyspnoea
Hyperhidrosis
Nausea
Symptomtext
About 5 minutes after recieving the vaccine, pt began sweating and was dizzy, out of breath, and nauseous. Symptoms resolved within 10 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Symptomtext
Systemic: Allergic: Difficulty Breathing-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 10.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Injection site swelling
Nausea
Tremor
Vision blurred
Symptomtext
Patient felt light headed, developed nausea, blurry vision and shakiness. Had some injection site swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- psoriatic arthritis
- Vorgeschichte
- psoriatic arthritis
- Andere Medikamente
- unknown
- Allergien
- gluten, eggs
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 09.08.2021
- Impfdatum
- 07.08.2021
- Beginn
- 08.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Migraine
Pyrexia
Vomiting
Symptomtext
Fever, vomiting, migraines
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Cymbals, lamictal, seroquil
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 09.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Asthenia
Fatigue
Flatulence
Headache
Injection site erythema
Injection site pain
Injection site swelling
Joint range of motion decreased
Mobility decreased
Musculoskeletal stiffness
Myalgia
Nausea
Pain
Photophobia
Symptomtext
5th August @3pm until 7th August 8am sore swollen red painful to touch or lift arm/injection site nausea 5th August (few hours After the shot) early hours 3am: abdominal cramps nausea weak feeling lots of gas and pain 6th August weak fatigued no more abdominal cramps but nauseous low energy levels through til 7th August 8th August : light sensitivity headaches muscle pains can?t put chin to chest area between scapulas extremely sore esp when moving neck. 9th symptoms have eased but still experiencing bouts of nausea and slight neck stiffness and fatigue and tiredness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Have no energy to even go to the doctors
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 08.08.2021
- Impfdatum
- 08.08.2021
- Beginn
- 08.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site hypoaesthesia
Injection site paraesthesia
Symptomtext
2:44pm pt said upper arm was tingling and numb surrounding injection site, resolved after a few minutes after applying an ice pack at 2:48pm to area, checked bp and pulse 2:49pm hr 114 bp 120/89, pt said she was nervous and later said dehydrated from playing softball yesterday, 2:52pm bp121/85 pulse 113, 2:56pm hr 113bp 137/82, 2:57pm 112/77 pulse 114, 3:08 pm 123/86 bp and 104 pulse- said was feeling fine and left
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 07.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Hypoaesthesia
Paraesthesia
Pyrexia
Symptomtext
Extreme chills, fever, headache, numbness and tingling in all 10 fingertips
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- TBI, back and neck issues
- Andere Medikamente
- None
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 06.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cold sweat
Dehydration
Dysphagia
Ear discomfort
Feeling hot
Thirst
Vision blurred
Symptomtext
pt went to the car and came back after 30 minutes and said she was feeling clamy and thirsty., we gave her some water. she said she was just getting hot. after about 15 more minutes she said the water was a little hard to swallow so we gave her benadryl 25mg. we watched and waited for an additional 20 minutes and she she was feeling better but then she said her eyes were getting blurry so we called 911. i was in the middle of taking bp when ems got there and took it and was 80/40. she then said her bp was 80/40 at dr's office that morning also ( she told me she had high blood pressure) . the ems thought she was dehydrated but she was having clogged ears so they took her to er by ambulance. she got onto the gurney on her own
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- high blood pressure diabetes per pt
- Vorgeschichte
- diabetes, high blood pressure per pt
- Andere Medikamente
- unknown
- Allergien
- none per pt
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 06.08.2021
- Impfdatum
- 04.08.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia oral
Paraesthesia oral
Symptomtext
Numbness/tingling sensation on the tip of the tongue and roof of mouth behind front teeth.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Phentermine Prozac
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 05.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dyspnoea
Nausea
Vaccination complication
Vomiting
Symptomtext
Patent had nausea, vomitting, shortness of breath, and dizziness ,,, adverse events occur a few minutes of getting shot. and adverse reaction lasted for 5 minutes. and after that she was feeling fine. And also patient said that adverse reaction may be due to low blood sugar.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 30.07.2021
- Impfdatum
- 30.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Dizziness
Dyspnoea
Pruritus
Vomiting
Symptomtext
Pharmacy gave vaccine to patient and right after few minutes patient said she she feeling dizzy so pharmacy put on her head and neck her ice pack and one tech stayed with patient then right after patient started itching, vomiting. Pharmacy called 911 right away. After vomit patient started shortness of breath. pharmacy stayed with patient till EMS came. Patient got severe reaction to vaccine. EMS took patient to hospital. patient was little better after EMS gave her nebulizer albuterol. Patient called around 4.27pm to update Pharmacy that she is doing ok and getting discharge. she mention that her blood pressure went up While EMS was taking her to hospital. she Also mention that she is really thankful Pharmacy staff for prompt action and saving her life.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 23.03.2023
- Impfdatum
- 28.09.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
Patient stated she started itching shortly after receiving the Covid vaccine. The next day she started itching all over her body. No rash noted. Nurse recommended that patient follows up with her doctor and go to the emergency room if she experiences any shortness of breath, throat swelling, or fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 08.12.2022
- Impfdatum
- 25.10.2021
- Beginn
- 10.06.2022
- Tage bis Beginn
- 228,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
COVID-19
Fatigue
Feeling abnormal
Headache
Nausea
Productive cough
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I was walking in the store, and I had to sit down before we got to the back of the store. I got a headache, fatigue, upset stomach, phlegmy cough, and nausea. I tested positive for COVID-19 at home. By the 12th I had a fever of 105 and I went to the doctor. They told me to take vitamin D3, vitamin C, zinc, benzonatate and TYLENOL PM. My fever went down to 104 for two days. I still have fatigue and feel bad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test, positive, 06/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- A-fib; High Blood Pressure
- Andere Medikamente
- Losartan; XARELTO; amlodipine; hydrochlorothiazide
- Allergien
- Radioactive dye
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 07.08.2021
- Beginn
- 11.08.2022
- Tage bis Beginn
- 369,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
Fall
Pyrexia
SARS-CoV-2 test positive
Surgery
Symptomtext
Pt presented to hospital post mechanical fall, status post surgery. pt tested for covid for fervers but other wise asymptomatic. once stable pt d/c to snf.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- gout, hypertension, hyperlipidemia, diabetes mellitus on insulin, diabetic neuropathy, coronary artery disease and CKD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Injection site erythema
Injection site pain
Injection site pruritus
Injection site warmth
Neck pain
Pain
Tendonitis
Symptomtext
At about 3PM on 10/27/2021, I received my first Moderna booster for COVID-19. About an hour and a half later, the injection site turned red and became itchy. I ran a temperature of 101 degrees. By the morning of 10/28/2021, there was a 4-to 5-inch radius around the site that was red, hot, and itchy. It itched for 6 days. By 10/29/2021, there was pain that extended from the right side of my neck to my right elbow. I had had tendonitis before, and it reminded me of this. The pain continues to the time of this writing. On 6/7/2022, I went to an orthopedist to be treated for a condition not related to the vaccine. While I was there, I asked them if anything could be done to also treat the pain in my neck and arm. The doctor advised that it sounded like I had tendonitis, and she gave me a cortisone injection in the right shoulder. The cortisone shot has helped, though it has not completely eliminated the pain, and the doctor has recommended exercises for me to do. I am to return on 7/19/2022 for a follow-up. I will also add that I received my second Moderna booster on 5/18/2022, and this exacerbated the pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypothyroidism; damage to both kidneys resulting from long-term NSAIDs use (mostly resolved)
- Andere Medikamente
- Gabapentin; tramadol; TYLENOL; levothyroxine; vitamin D.
- Allergien
- Penicillin; codeine; sulfa drugs; LEVAQUIN; cat dander; pollen; grass; mold.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 06.04.2021
- Beginn
- 16.02.2022
- Tage bis Beginn
- 316,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Catheter placement
Dizziness
Headache
SARS-CoV-2 test positive
Symptomtext
Pt presents to ER via EMS with c/o dizziness 2/16. Pt admitted from ed, pt vital signs stable, pt oriented to room and unit, pt received dinner, tele monitor in place pt in SR, pt denies pain. COVID positive 2/16. Pt is aox4, on RA not in acute distress, c/o headache, with ongoing IV fluid infusing well, external cath in placed 2/19. Patient is A&O x 4. Able to sit up in a chair with two person assist. On room air. No complications 2/21. 5/23 pt denies any new c/o., denies any SOB, CP, N/V/D or abdominal pain. Discharged on 2/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- 8,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity (BMI 30-39.9)
- Andere Medikamente
- acyclovir (ZOVIRAX) 400 MG PO Tab, acyclovir (ZOVIRAX) 400 MG PO Tab amLODIPine (NORVASC) 5 MG PO Tab atorvastatin (LIPITOR) 40 MG PO Tab dexamethasone (DECADRON,HEXADROL) 4 MG PO Tab furosemide (LASIX) 20 MG PO Tab ixazomib (Ninlaro) 4 MG
- Allergien
- Benadryl, Tessalon Perles
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 11.10.2021
- Beginn
- 21.02.2022
- Tage bis Beginn
- 133,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Cyanosis
Dizziness
Dysgeusia
Feeling cold
Headache
Malaise
Nausea
Respiratory tract congestion
SARS-CoV-2 test positive
Taste disorder
Symptomtext
Tested positive for COVID 02/21/22. Headache and congestion, coughing. The symptoms weren't bad. It's hard to tell how long they lasted because I've been sick since I got COVID. Mostly has been chronic nausea which can't get over. Now there is a constant bitter taste in my mouth, and everything tastes like poison, I've had light-headiness, my finger and patch on my face on a scar I had surgery on turned blue whenever I'm cold. I've had chills for a long while.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- CT Scan scheduled on 04/27/2022, COVID test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Sarcoidosis - Autoimmune illness, High Blood Pressure
- Andere Medikamente
- Azathioprine, Losartan
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Fatigue
Malaise
Pain
Pain in extremity
Symptomtext
Chills, body aches, very sore arm, generalized malaise, fatigue for 24 hours, resolved between 24-48 hours after rest Then was positive for Covid 19, (omicron), 12/31/2021. Symptoms, constant cough, fatigue. Received Sotrovimab on 12/31/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, hypothyroidism, type 2 diabetes, high cholesterol
- Andere Medikamente
- Tylenol after the vaccine, Prescription medications: levothyroxine, metformin, triamterene/HCTZ, vascepa, Coq10, vitamin D, symbicort, livalo, Xolair, prolix, ventolin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 19.02.2021
- Beginn
- 05.03.2021
- Tage bis Beginn
- 14,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Feeling hot
Pruritus
Urticaria
Symptomtext
Face begins to get hot, red, and welts appear. This causes my face to itch significantly. Happens weekly at least once but sometimes multiple times. Goes away within an hour.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- -
- Allergien
- Seasonal allergies, dogs & cats, dust.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 01.09.2021
- Beginn
- 20.01.2022
- Tage bis Beginn
- 141,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On January 20, 2022 I had a runny nose that turned into a cough no fever. I experienced fatigue and I was tired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID (results positive)
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol, Avar
- Allergien
- Penicillin, Cephalosporins
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 02.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Fatigue
Headache
Malaise
Myalgia
Nausea
Symptomtext
Diarrhea; feel off, strange / feeling not myself; Nausea; sore arm,; fatigue; mild headache / dull headache; This spontaneous case was reported by a consumer and describes the occurrence of DIARRHOEA (Diarrhea), MALAISE (feel off, strange / feeling not myself), MYALGIA (sore arm,), FATIGUE (fatigue) and HEADACHE (mild headache / dull headache) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included Multivitamin. On 02-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Aug-2021, the patient experienced MYALGIA (sore arm,), FATIGUE (fatigue) and HEADACHE (mild headache / dull headache). On an unknown date, the patient experienced DIARRHOEA (Diarrhea), MALAISE (feel off, strange / feeling not myself) and NAUSEA (Nausea). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. On 03-Aug-2021, MYALGIA (sore arm,) and FATIGUE (fatigue) had resolved. At the time of the report, DIARRHOEA (Diarrhea), MALAISE (feel off, strange / feeling not myself) and NAUSEA (Nausea) outcome was unknown and HEADACHE (mild headache / dull headache) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient stated that he went to his doctor and they advised him to take Ibuprofen and drink fluid. Patient took Tylenol but it did not help that much, and patient is only Multivitamin as his regular medication.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Multivitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 05.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Myalgia
Peripheral swelling
Vaccination site pain
Vaccination site swelling
Symptomtext
swelling in arm; chills; body ache/body is starting to hurt; joint pain; Vaccination site swelling; Vaccination site pain; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (swelling in arm), CHILLS (chills), MYALGIA (body ache/body is starting to hurt), ARTHRALGIA (joint pain) and VACCINATION SITE SWELLING (Vaccination site swelling) in a 34-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 05-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced PERIPHERAL SWELLING (swelling in arm), CHILLS (chills), MYALGIA (body ache/body is starting to hurt), ARTHRALGIA (joint pain), VACCINATION SITE SWELLING (Vaccination site swelling) and VACCINATION SITE PAIN (Vaccination site pain). At the time of the report, PERIPHERAL SWELLING (swelling in arm), CHILLS (chills), MYALGIA (body ache/body is starting to hurt), ARTHRALGIA (joint pain), VACCINATION SITE SWELLING (Vaccination site swelling) and VACCINATION SITE PAIN (Vaccination site pain) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 02.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Fatigue
Hiccups
Myalgia
Pain in extremity
Pyrexia
Symptomtext
Uncontrollable hiccups; Arm pain; Muscle pain; Chills; Fever; Tiredness; Skin redness; This spontaneous case was reported by a consumer and describes the occurrence of ERYTHEMA (Skin redness), HICCUPS (Uncontrollable hiccups), PAIN IN EXTREMITY (Arm pain), MYALGIA (Muscle pain) and CHILLS (Chills) in a 46-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included COPD. On 02-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Aug-2021, the patient experienced ERYTHEMA (Skin redness), PAIN IN EXTREMITY (Arm pain), MYALGIA (Muscle pain), CHILLS (Chills), PYREXIA (Fever) and FATIGUE (Tiredness). On 04-Aug-2021, the patient experienced HICCUPS (Uncontrollable hiccups). At the time of the report, ERYTHEMA (Skin redness), HICCUPS (Uncontrollable hiccups), PAIN IN EXTREMITY (Arm pain), MYALGIA (Muscle pain), CHILLS (Chills), PYREXIA (Fever) and FATIGUE (Tiredness) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant product information was provided. No treatment information was provided. Most recent FOLLOW-UP information incorporated above includes: On 29-Dec-2021: Follow up received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COPD.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 02.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Peripheral swelling
Symptomtext
Left arm swelled up to the "size of a soda can" / left arm is still swollen; Normal aches and pain; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (Left arm swelled up to the "size of a soda can" / left arm is still swollen ) and MYALGIA (Normal aches and pain) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. Concurrent medical conditions included Diabetes. Concomitant products included METFORMIN for Diabetes. On 02-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Aug-2021, the patient experienced PERIPHERAL SWELLING (Left arm swelled up to the "size of a soda can" / left arm is still swollen ) and MYALGIA (Normal aches and pain). At the time of the report, PERIPHERAL SWELLING (Left arm swelled up to the "size of a soda can" / left arm is still swollen ) had not resolved and MYALGIA (Normal aches and pain) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diabetes
- Vorgeschichte
- -
- Andere Medikamente
- METFORMIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 01.12.2021
- Beginn
- 28.01.2022
- Tage bis Beginn
- 58,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Flatulence
Herpes zoster
Nausea
Rash
Symptomtext
Nauseated, it felt like gas that wouldn't go away, felt in back and stomach on the 28th of January that lasted all weekend. Then on the 31st about 6pm in evening, I noticed the rash forming on the front part under my breast on left wrapped around to my back. I then went to the doctor on that Tuesday afternoon 02/01/2022 and was diagnosed with shingles. I was prescribed Valtrex 3 x daily and Gabapentin for pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- 1. Diabetes 2. Hypothyroidism 3. Breast Cancer (In remission) 4. Cervical Cancer (In remission) 5. Asthma 6. High Cholesterol
- Andere Medikamente
- 1. Synthroid 50mcg 1 2. Jardiance 25mg 1x daily 3. Lipitor 10mg 1xdaily 4. Zyrtec 10mg daily 5. Lexapro 10mg daily 6. Arimidex 1mg tablet daily 7. Cingular 10mg daily 8. HCTZ 25mg daily 9. Metformin 500 mg 2x daily 10. Aspirin 81mg daily
- Allergien
- 1. Wellbutrin 2. Lisinopril 3. Seasonal
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 05.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Sore arm; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Sore arm) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 05-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (Sore arm). At the time of the report, PAIN IN EXTREMITY (Sore arm) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. No concomitant and treatment drugs were reported. No treatment information was reported. Reporter stated that his wife got the booster dose too early, because of the negligence of the pharmacist. It was 24 days before the 5 months details included Booster dose on 08Jan2022 ,Lot - 033H21A. This case was linked to MOD-2022-467313, MOD-2022-467315 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 13.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Urticaria
Symptomtext
I developed severe hives and itching in random spots of my body. Was put on a 10 day course of steroids and still no relief after the steroids
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Went to see the Allergist Dr and she did a hives test and based on my hysterectomy of not having hives ever then stating that she has had several patients that developed hives from the covid/booster shot. This is what is happening to me.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Statin meds,, sulfa,, zithromax
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 03.09.2021
- Beginn
- 05.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Asthenia
Chills
Cough
Depression
Diarrhoea
Fatigue
Feeling of despair
Grip strength decreased
Inflammation
Influenza
Influenza like illness
Laboratory test
Muscular weakness
Myalgia
Red blood cell sedimentation rate normal
Sinus disorder
Symptomtext
He got his vaccine, had flu like symptoms for the first 2 days, chills, muscle pain. The 2nd or 3rd day was coughing and sneezing for 2-3 days. The 5th day was severe diarrhea. Then he started to feel better on the 6th day and then on the 7th day he felt fine and then on the 11th day the symptom started all over again, the exact same way and the symptoms continued in a cycle. He then saw his PCP who started doing tests and have been doing testing since. He asked him to prescribe him for inflammation/joint pain and he prescribed Ibuprofen for that. His doctor did prescribe antibiotics thinking it was a bacterial infection, but the antibiotics didn't help and tested him again and it was negative. He is now having coughing, sneezing, sinus but only for a few days and very mild and goes away, and then cycles back around again every couple of days. It stopped being 7 days of flu about the 12th time and then stops for a few days and then continues. He has weakness of his legs, cannot grasp things like a gallon of milk is too heavy, has weakness and fatigue. He feels as if his body has inflammation but his SED rate came back normal, and wonders what is going on and did not have any of this before the vaccine. He did have a neck injury in the past, was jogging and getting back in health and loosing weight and since the vaccine has severe arthritis and is depressed and desperate and feels that he won't be here if there is no improvement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Multiple as above.
- Aktuelle Erkrankungen
- With first vaccine his body went into shock, threw up and dizziness with almost passing out, and then had cold like symptoms from the first vaccine that lasted for about a month.
- Vorgeschichte
- None.
- Andere Medikamente
- Gabapentin 300 mg, Adderall XR 20 mg, Hydrocodone 5/325.
- Allergien
- Peppers, peanuts, soy beans.
- Vorherige Impfungen
- Filed report for first vaccine, ID#1536470 When he gets a flu shot he sometimes gets the flu 1-2 times in the last 20-30 flu sh
- Staat
- NC
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 27.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dry skin
Laboratory test
Pruritus
Rash pruritic
Sleep disorder
Symptomtext
Severe itchy skin, itchy bumps, itch is so bad it wakes me up in the middle of the night, the scratching has cause bruising and lesions on my skin. I was told from the PCP that I had "severe dry skin." Changed soaps, detergents and lotions as directed with no relief. Dermatologists recommended a steroid cream and Allegra x 1 in the morning and Xyzal x 1 at night, with no relief. Symptoms started days after receiving the 2nd dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Scratch tests, Scabies test, all negative
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 23.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
Back pain
COVID-19
Full blood count normal
Headache
Malaise
Pyrexia
Rash
SARS-CoV-2 test positive
Symptomtext
After I got the booster, 11/23/2021- I got a rash all over my chest, that evening. It got worse when I got symptomatic with COVID-19 and it just cleared up in the last week. I got a rash after my 1st Moderna vaccine on my back. On 11/27/2021-I thought I pulled a muscle in my back, I was having back pain. I had fever, headache, no taste and smell. It all stayed in my head though, it did not go into my chest. On 11/29/2021-At the Hospital -I tested positive for COVID-19 and I received the monoclonal antibodies on that same day. They also gave me a dexamethasone injection and a Zofran. And I had some prescription cough medicine. I am recovered. I still have some of my fatigue and my taste isn't right. Note: I did receive the flu vaccine sometime in October, but I don't remember when.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- 11/29/2021- COVID-19 test- positive; CBC- was fine
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- LEXAPRO; AMBIEN; hormone patch
- Allergien
- No
- Vorherige Impfungen
- All vaccines make my arm extremely sore.
- Staat
- FL
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 01.09.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 34,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest discomfort
Feeling hot
Malaise
SARS-CoV-2 test negative
Symptomtext
BP: 151/100 Pulse 125 Resp:20 Temp 98.6 Weight 203 Height 5' 10.5" BMI: 28.751 02SAT 98% Tightness in chest and overall unwell feeling, presented myself to urgent care and was told to go to nearest hospital. Arrived at Hospital where multiple vials of blood were taken for tests, I was put on some sort of liquid iv and a few hrs later I was released. Since that time, I am always running hot, is the only way I can describe it. I can have the AC on in the house and it be 68 degrees and Im not cold but wife is freezing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Covid negative test x2 were done and bayonet point hospital has labs
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- lamotrigine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 22.08.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood test
Burning sensation
Computerised tomogram
Fatigue
Hypoaesthesia
Magnetic resonance imaging
Nervous system disorder
Symptomtext
Pt. states that after receiving the 2nd dose of Moderna 08/22/2021, started experiencing symptoms that evening of burning sensation throughout the body, fatigue, numbness, weakness lasting 2 weeks. Primary visit referral for Neurologist. Prescribed Lyrica for nervous system. Pt. still experiencing symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Cat-Scan 09/2021 Blood Work 09/2021 MRI 09/2021
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Tylenol
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 18.09.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Deafness
Dizziness
Fatigue
Injection site pain
Injection site swelling
Insomnia
Lethargy
Lymphadenopathy
Nausea
Pain
Pruritus
Pyrexia
Tinnitus
Symptomtext
Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Mild, Systemic: Joint Pain-Medium, Systemic: Lymph Node Swelling-Mild, Systemic: Nausea-Mild, Systemic: Tinnitus-Severe, Systemic: Unable to Sleep-Medium, Additional Details: -Dizziness occured 3 minutes after vaccination. At first this was a frequent occurence and now it happens sometimes (rarely). -Ring in my ears - Consistent; stronger as the day goes by. Results in me being very tired. ENT has confirmed slight hearing loss and tinnitus. He has classified this as permanent damage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 23.08.2021
- Beginn
- 24.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Aldolase normal
Anti-ganglioside antibody negative
Antinuclear antibody negative
Asthenia
Blood test normal
Blood thyroid stimulating hormone normal
Borrelia test negative
C-reactive protein normal
Cognitive disorder
Complement factor C3
Complement factor C4
Differential white blood cell count normal
Discomfort
Exercise tolerance decreased
Full blood count normal
Gait disturbance
Head discomfort
Headache
Symptomtext
I received the first dose of Moderna in March 2021. After that shot, I had difficulty walking for two weeks. When I tried to move forward, the center of my back and my sides felt very strained as if I was pulling a bus behind me. The symptoms completely went away after those two weeks. I decided not to get the second vaccine. However, around August 20, 2021, it was mandated the vaccine for teachers. My doctor refused to give me an exemption, so in order to save my carreer, I got the second dose. That was 17 weeks ago, and I have been unable to work since then. Within a day or two of the second vaccine, I had a much more severe reaction. The vaccine devastated my nervos system. It was 3 months before I could begin to walk beyond 20-30 steps. Something was wrong deep inside my spinal cord. It wasn't an injury because I could stretch without any muscle pain. During that time, I had concussion-like symptoms that kept me sitting in a dark room with sunglasses on. I could not handle any screentime or flashing lights of any kind. I could not ride in a car because the movement and stimulation was intolerable. My eyes couldn't focus from one thing to another. I had continuous mild eye headaches. When I tried to walk, I had intense pressue on the back of my head and neck. It was terrible strain on my spinal cord to walk. After a handful of slow steps, I felt as if my brain wouldn't communicate with my legs to tell them to move forward. I was unable to strain my body in any way. I could not cut vegetables, couldn't carry objects without cradling them to my chest. I could not push/pull a vaccuum cleaner. I was extremely sick and weak for those first 3 months. I was unable to work, to drive, to exercise, or to take care of my household. After exerting myself or using my eyes, I had to sleep in order to relieve the discomfort and ease the cognitive stress that I felt from using my eyes. In the fourth month, my symptoms began to subside. I have slowly increased the distance that I can walk and the light sensitivity has eased. I am just beginning to handle the stimulation of being in a car and in public places. I can drive short distances, but my eyes are very strained. I am a fourt grade teacher and I have not even met my class this year. 09/03/2021 - all tests came back normal Complete Blood Count, with Differential - Comprehensive Metabolic Panel; Future - TSH Reflex Free T4; Future - Comprehensive Metabolic Panel - TSH Reflex Free T4 - Ganglioside Gm-1 Antibody, IgG, IgM 09/23/2021 - Brain MRI with Contrast - results were normal 10/01/2021 - Emergency Room Visit Blood Tests - all came back negative or in normal ranges Miscellaneious Test, ARUP Sedimentation Rate C3 Complement C$ Complement C-Reative Protein JO-1 Antibody Aldolase, Seru ANA, IGG by ELISA w REflex to HEP-2 Lyme Disease Giemsa Stain 10/19/2021 - Neurological exam with Dr. - results were normal; adverse neurological effects from vaccine should diminish over time I was given a 5-day steroid pack. It did not have any affect on me other than sleeplessness. 11/1/2021 - Dr., Rheumatologist - All tests came back normal; I do not have an autoimmune disease
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 09/23/2021 - Complete Blood Count, with Differential - Comprehensive Metabolic Panel; Future - TSH Reflex Free T4; Future - Comprehensive Metabolic Panel - TSH Refl
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Vtamins C and D, zinc
- Allergien
- none
- Vorherige Impfungen
- Approximately 15-20 years ago, I had my only flu shot and I felt unwell for quite a while.
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 13.09.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Rash
Symptomtext
a rash around hips and buttocks (since first dose) along with a headache; headache; This spontaneous case was reported by a consumer and describes the occurrence of RASH (a rash around hips and buttocks (since first dose) along with a headache) and HEADACHE (headache) in a 60-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 13-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced RASH (a rash around hips and buttocks (since first dose) along with a headache) and HEADACHE (headache). The patient was treated with CALAMINE, GLYCEROL, ZINC OXIDE (CALAMINE LOTION) for Adverse event, at an unspecified dose and frequency; PREDNISONE for Adverse event, at an unspecified dose and frequency; MENTHOL (GOLD BOND MEDICATED ORIGINAL STRENGTH BODY POWDER) for Adverse event, at an unspecified dose and frequency and PARAFFIN (MOISTURIZER) for Adverse event, at an unspecified dose and frequency. At the time of the report, RASH (a rash around hips and buttocks (since first dose) along with a headache) and HEADACHE (headache) had not resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. No concomitant medication was reported. Patient took second dose of Moderna COVID-19 Vaccine on 11-OCT-2021 in left arm (Lot number 040C21A).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 09.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pain
Pain in extremity
Symptomtext
Muscle pain, arm pain that is continuous, generalized muscle aches and pains to the whole body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Recent fall without major injury
- Vorgeschichte
- Breast CA Insomnia Cataracts A fib Diverticulitis Pacemaker placement
- Andere Medikamente
- Product SIG Miralax 17 gram/dose 1 scoop powder by mouth once a day biotin 1 mg 1 capsule by mouth once a day cyanocobalamin (vitamin B-12) 1,000 mcg 1 capsule by mouth once a day magnesium amino acid chelate 100 mg 2 1/2 tablet by mouth on
- Allergien
- Codeine Intolerance to prednisone
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 29.10.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Full blood count normal
Pruritus
Urticaria
Symptomtext
Pt developed hives and itching 10 days after 3rd dose of Moderna. No problem with dose 1 or 2 of Moderna. Hives are all over 1-6in in diameter, triggers by touch, meals, and time of day. Treated to initially with OTC hydrocortisone and antihistamines. He saw employee health NP and was treated with methylprednisolone and hydroxyzine which reduced symptoms to 1/3. He is now following with Dr. who has treated him with Zyrtec and Prednisone and symptoms are continuing to improved but still present. He also has flares of diverticulitis and is scheduled for gal bladder surgery. Dr. has indicated to him that hives may be a combo of gut inflammatory processes and the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- see above. CBC WNL. Additional allergy testing is being considered by physician.
- Aktuelle Erkrankungen
- diverticulitis, planned gal bladder removal
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 17.09.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Abdominal pain upper
Body temperature
Diarrhoea
Disturbance in attention
Fatigue
Feeling abnormal
Headache
Illness
Lethargy
Nausea
Neck pain
Nightmare
Pyrexia
Somnolence
Vaccination complication
Symptomtext
I am sick; felt that I was going to vomit; I had an upset stomach; extremely tired; having horrible nightmares every night to the point I wake up in fright 10 times a night./Horrible, bizarre nightmares; severe neck pain/neck pain for 7 days on his left side; Low grade fever; Headache; felt foggy / had trouble focusing/he just didn't feel right; lethargic; Vaccination related malaise; stomach aches/stomach cramps; Diarrhea; couldn't stay awake/the next day he did not wake up until noon/Slept for three days; tiredness to the point I slept almost 3 straight days / only getting out of bed to go to the bathroom and try to eat./ extremely tired/He couldn't believe how tired he was and he even missed work; severe headache; had trouble focusing; This spontaneous case was reported by a consumer and describes the occurrence of LETHARGY (lethargic), VACCINATION COMPLICATION (Vaccination related malaise), ABDOMINAL PAIN UPPER (stomach aches/stomach cramps), DIARRHOEA (Diarrhea) and FEELING ABNORMAL (felt foggy / had trouble focusing/he just didn't feel right) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 040D21A and 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Penicillin allergy. On 17-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Oct-2021 at 5:30 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 15-Oct-2021, the patient experienced ABDOMINAL PAIN UPPER (stomach aches/stomach cramps), DIARRHOEA (Diarrhea), HEADACHE (severe headache) and FATIGUE (tiredness to the point I slept almost 3 straight days / only getting out of bed to go to the bathroom and try to eat./ extremely tired/He couldn't believe how tired he was and he even missed work). 15-Oct-2021, the patient experienced SOMNOLENCE (couldn't stay awake/the next day he did not wake up until noon/Slept for three days). In October 2021, the patient experienced DISTURBANCE IN ATTENTION (had trouble focusing). On 16-Oct-2021, the patient experienced LETHARGY (lethargic), VACCINATION COMPLICATION (Vaccination related malaise) and FEELING ABNORMAL (felt foggy / had trouble focusing/he just didn't feel right). On 09-Nov-2021, the patient experienced PYREXIA (Low grade fever). On 12-Nov-2021, the patient experienced NECK PAIN (severe neck pain/neck pain for 7 days on his left side). On 15-Nov-2021, the patient experienced NIGHTMARE (having horrible nightmares every night to the point I wake up in fright 10 times a night./Horrible, bizarre nightmares). In November 2021, the patient experienced HEADACHE (Headache). On 22-Nov-2021, the patient experienced ABDOMINAL DISCOMFORT (I had an upset stomach) and NAUSEA (felt that I was going to vomit). 22-Nov-2021, the patient experienced FATIGUE (extremely tired). On 26-Nov-2021, the patient experienced ILLNESS (I am sick). The patient was treated with IBUPROFEN in November 2021 for Fever, at an unspecified dose and frequency. In October 2021, HEADACHE (severe headache) had resolved. On 17-Oct-2021, SOMNOLENCE (couldn't stay awake/the next day he did not wake up until noon/Slept for three days) had resolved. On 18-Oct-2021, FATIGUE (tiredness to the point I slept almost 3 straight days / only getting out of bed to go to the bathroom and try to eat./ extremely tired/He couldn't believe how tired he was and he even missed work) had resolved. On 21-Oct-2021, ABDOMINAL PAIN UPPER (stomach aches/stomach cramps) and DIARRHOEA (Diarrhea) had resolved. On 19-Nov-2021, NECK PAIN (severe neck pain/neck pain for 7 days on his left side) had resolved. On 25-Nov-2021, ABDOMINAL DISCOMFORT (I had an upset stomach), NAUSEA (felt that I was going to vomit) and FATIGUE (extremely tired) had resolved. At the time of the report, LETHARGY (lethargic), VACCINATION COMPLICATION (Vaccination related malaise), FEELING ABNORMAL (felt foggy / had trouble focusing/he just didn't feel right), NIGHTMARE (having horrible nightmares every night to the point I wake up in fright 10 times a night./Horrible, bizarre nightmares), ILLNESS (I am sick), PYREXIA (Low grade fever) and HEADACHE (Headache) had not resolved and DISTURBANCE IN ATTENTION (had trouble focusing) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 09-Nov-2021, Body temperature: low grade (High) Low grade fever. Weight of the patient was given as 175 (no units mentioned). The patient was taking vitamins. The patient got second Moderna shot on October 15th at 5:30 from the vaccination facility. The next day he did not wake up until noon, he usually sleeps for 6 to 7 hours and within 12 hours of the second shot he developed a severe headache and tiredness to the point he slept almost 3 straight days, only getting out of bed to go to the bathroom and try to eat. He even missed work. He stated he just did not feel right. The patient also developed stomach aches and diarrhea. The symptoms slowly went away over the next 7 days. For the following week he could function but felt foggy and had trouble focusing. He stated by the 4th or 5th week after the injection he developed severe neck pain for 7 days on his left side, a headache and low grade fever. The neck pain and headache went away after 8 days but patient still had a fever along with new symptoms. The patient had been running a low grade fever for the past three weeks. The patient tried ibuprofen but fever not recovered. From 22nd November to the 25th November2021, patient became extremely tired, could not stay awake and he had an upset stomach, and felt that he was going to vomit. Patient also had horrible nightmares every night to the point he woke up in fright 10 times a night. The patient still had a low grade fever and a headache and was felt foggy and out of it. When asked if he has consulted with a physician the patient stated that he did not feel as if he was in a financial position to go to a doctor. The patient stated that before taking moderna vaccine he had zero underlying health conditions and felt great. The patient had a lot of energy, was extremely focused and sharp. This case was linked to MOD-2021-399953 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 26-Nov-2021: Significant follow up contains additional events, patients last name and email address. On 29-Nov-2021: Significant follow up contains patient's demographics and reporting details, additional event and details of 1st dose of vaccine. On 06-Dec-2021: Follow up received on 06-Dec-21 contained significant information Patient height, weight, ethnicity, Medical history, dose 1 and 2 details and event outcomes were updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211109; Test Name: body temperature; Result Unstructured Data: Low grade fever
- Aktuelle Erkrankungen
- Penicillin allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 17.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Pain in extremity
Symptomtext
Some arm pain; Headache; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Some arm pain) and HEADACHE (Headache) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 17-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Sep-2021, the patient experienced PAIN IN EXTREMITY (Some arm pain) and HEADACHE (Headache). On 22-Sep-2021, HEADACHE (Headache) had resolved. At the time of the report, PAIN IN EXTREMITY (Some arm pain) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications included only vitamins. No treatment medications were reported. This case was linked to MOD-2021-398800 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lip swelling
Pruritus
Symptomtext
VACCINE WAS RECEIVED AT THE PHARMACY IN EARLY AFTERNOON AT THE PHARMACY. APPROXIMATELY 9PM SHE STARTED TO EXPERIENCE LIPS SWELLING AND ITCHING SKIN. TREATED WITH BENADRYL 50MG [2 X 25MG CAPSULES] AND REPEATED AT 2AM. REACTION SUBSIDED BY 3AM. PATIENT REFUSED TO USE EPI PEN [WHICH SHE HAS A PRESCRIPTION] AND REFUSED TO GO TO EMERGENCY ROOM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- HYPERTENSION EARLY ONSET DEMENTIA INCONTINENCE HYPERLIPIDEMIA
- Andere Medikamente
- PANTOPRAZOLE, OXYBUTYNIN, LOSARTAN, ATORVASTATIN
- Allergien
- CODEINE INSECT BITES PEANUT
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Fatigue
Induration
Skin warm
Symptomtext
After getting the booster I was a bit fatigue on Friday night, Saturday night I went to sleep at 10pm and woke up at 12noon. Around that same night and noticed my arm was hot, and hard.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- I have a vary rare form of cancer in 2011 and I have gotten chemotherapy I have anxiety and seasonal allergies I am on immune therapy for indoor and outdoor allergies.
- Andere Medikamente
- I was taking prescribed medication.
- Allergien
- Clindamycin Citroma Biaxin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Rash
Symptomtext
Patient complained of "COVID Arm" with redness and rash that traveled down her arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 05.11.2021
- Impfdatum
- 07.08.2021
- Beginn
- 08.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test abnormal
Hypoaesthesia
Infection
Injection site inflammation
Injection site pain
Injection site reaction
Injection site swelling
Magnetic resonance imaging abnormal
Muscle spasms
Neuralgia
Pain
Scoliosis
White blood cell count increased
X-ray abnormal
Symptomtext
There was pain, swelling and inflammation at the injection site. Went to the Dr when the swelling was a little bigger than a plumb. They prescribed antibiotics and the infection seemed to clear up, but I was/am still experiencing inflammation and a burning nerve pain in the area of the injection, that radiates down my arm. If I push the use of that arm the pain becomes almost unbearable, and I experience numbness and muscle spasms all the way to my fingers. Upon further diagnosis (X-ray and MRI) I was diagnosed with Scoliosis, which wasn't a pre-existing condition as far as anyone was aware.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site inflammation
- Hospital-Tage
- -
- Labordaten
- Blood work showed elevated white blood cell count, and high kidney enzymes on October 6 2021. A shoulder X-ray and Spinal MRI were done on November 4, 2021 which showed the Scoliosis.
- Aktuelle Erkrankungen
- Agoraphobia, MDD, Obesity
- Vorgeschichte
- Obesity, Agoraphobia, MDD, Unspecified Fatigue
- Andere Medikamente
- Aspirin, Lisinopril
- Allergien
- Morphine, Buspar, Silver Sulfidide, Red Food coloring
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 05.11.2021
- Impfdatum
- 03.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site swelling
Injection site warmth
Type IV hypersensitivity reaction
Symptomtext
Delay site reaction 8 days after vaccine was given. Raised 2" x 2" circle on the arm at the injection site, red with fever in it, lasted 3-4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High cholesterol High Blood Pressure
- Andere Medikamente
- Losartan Atorvastatin Cialis
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 09.06.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Arthralgia
Asthenia
Laboratory test normal
Symptomtext
amenorrhea since vaccine administration joint pain and generalized weakness since vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- advised to see pcp for r/o conditions r/t joint pains. hormonal labs to rule out asymptomatic premature menopause
- Aktuelle Erkrankungen
- denies
- Vorgeschichte
- denies
- Andere Medikamente
- denies
- Allergien
- denies
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Nodule
Pain in extremity
Peripheral swelling
Pyrexia
Symptomtext
Patient reports swelling of the arm and a knot directly under the armpit happening about 6 hours after vaccine. She now has bruising down her side and at ribcage to bra level. She also had a mild fever after shot. Patient is reporting this 6 days later and still has moderate bruising as well as pain and swelling of the arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Vertigo
Symptomtext
Fatigue initially, subsided after 24 hours. Approximately 48 hours after the vaccinations vertigo began and is not consistent. Vertigo happens when laying down, getting up too quickly, or excessive movement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism, depression, anxiety
- Andere Medikamente
- Levothyroxine (50mg), sertraline (150mg), albuterol (PRN), Flovent (PRN), Benadryl (PRN), Claritin (PRN), Flonase (daily)
- Allergien
- Allergies to grasses & dander. No known food products.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Developed painful headache behind eyes 1 hour after vaccine and headache has persisted 28 days. Improves with over the counter pain medication but does not resolve. No other symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unnknown
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Fatigue
Pain in extremity
Pyrexia
Symptomtext
Received vaccine 10-27-21 at 10:20 a.m. Sore arm about an hour later. Woke with chills and fever 10-28-21 at 1:00 a.m. Lasted about an hour. Took ibuprofen. Tired and had slight fever during the day of 10-28-21. Took ibuprofen. Reaction was similar, but not as bad, as the reaction I had to 2nd Moderna vaccine on 4-6-21, which I also reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Nasal allergies
- Andere Medikamente
- Paroxetine 20 mg once per day Famotidine 20 mg once per day Flonase nasal spray once per day Womens Multivitamin once per day Fiber Choice fiber supplement 2 tablets once per day
- Allergien
- None
- Vorherige Impfungen
- Moderna 2nd vaccine, 4-6-21, similar reaction but worse
- Staat
- TN
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 26.08.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 49,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Diarrhoea
Faeces discoloured
Symptomtext
black stool; diarrhea that is watery and charcoal colored/diarrhea very frequent; not eating; This spontaneous case was reported by a consumer and describes the occurrence of FAECES DISCOLOURED (black stool), DIARRHOEA (diarrhea that is watery and charcoal colored/diarrhea very frequent) and DECREASED APPETITE (not eating) in an 89-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 045C21A and 939902) for COVID-19 vaccination. No Medical History information was reported. Concomitant products included HYDROCHLOROTHIAZIDE and PRAVASTATIN for an unknown indication. On 26-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 14-Oct-2021, the patient experienced FAECES DISCOLOURED (black stool), DIARRHOEA (diarrhea that is watery and charcoal colored/diarrhea very frequent) and DECREASED APPETITE (not eating). The patient was treated with BISMUTH SUBSALICYLATE (PEPTO BISMOL [BISMUTH SUBSALICYLATE]) for Adverse event, at an unspecified dose and frequency. At the time of the report, FAECES DISCOLOURED (black stool), DIARRHOEA (diarrhea that is watery and charcoal colored/diarrhea very frequent) and DECREASED APPETITE (not eating) had not resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No Medical History information was reported.
- Andere Medikamente
- HYDROCHLOROTHIAZIDE; PRAVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 22.10.2021
- Impfdatum
- 30.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Headache
Lymph node pain
Lymphadenopathy
Pain
Vomiting
Symptomtext
Severe pain and welling of lymph nodes located in arm pit of vaccinated arm - lasted 5 days. Heavy metallic taste in mouth. Vomiting, headache, body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 20.10.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Illness
Product dose omission issue
Pyrexia
Symptomtext
Patient missed the 2nd dose window; Sick for a day; Fever; This spontaneous case was reported by a pharmacist and describes the occurrence of ILLNESS (Sick for a day), PYREXIA (Fever) and PRODUCT DOSE OMISSION ISSUE (Patient missed the 2nd dose window) in a 20-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 20-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Aug-2021, the patient experienced PRODUCT DOSE OMISSION ISSUE (Patient missed the 2nd dose window). On an unknown date, the patient experienced ILLNESS (Sick for a day) and PYREXIA (Fever). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. On 20-Aug-2021, PRODUCT DOSE OMISSION ISSUE (Patient missed the 2nd dose window) had resolved. At the time of the report, ILLNESS (Sick for a day) and PYREXIA (Fever) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 17.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 16.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Hypersomnia
Lethargy
Pain
Pyrexia
Symptomtext
Severe Fever. Body Aches. Chills. Lethargy (Slept most of the next day and most of the following day) Severe headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 04.09.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cold sweat
Dizziness
Feeling abnormal
Malaise
Pyrexia
Vomiting
Symptomtext
still not feeling well/doesn't feel well; feels miserable from it; little lightheaded; got a little clammy; throwing up/throwing up for 8-10 hours; low-grade fever; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (still not feeling well/doesn't feel well), FEELING ABNORMAL (feels miserable from it), DIZZINESS (little lightheaded), COLD SWEAT (got a little clammy) and VOMITING (throwing up/throwing up for 8-10 hours) in a 20-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 061E22A and 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 04-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Oct-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced MALAISE (still not feeling well/doesn't feel well), FEELING ABNORMAL (feels miserable from it), DIZZINESS (little lightheaded), COLD SWEAT (got a little clammy), VOMITING (throwing up/throwing up for 8-10 hours) and PYREXIA (low-grade fever). At the time of the report, MALAISE (still not feeling well/doesn't feel well), FEELING ABNORMAL (feels miserable from it), DIZZINESS (little lightheaded), COLD SWEAT (got a little clammy), VOMITING (throwing up/throwing up for 8-10 hours) and PYREXIA (low-grade fever) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Treatment informations were reported. This case was linked to MOD-2021-346807 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 26.08.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Myalgia
Pyrexia
SARS-CoV-2 test
Symptomtext
Had a 100 degrees F fever ongoing until today/in the morning he will have a fever of 99.1 ranging to 101 degrees F by evening; Chills when traveling on the plane; Felt achy; Fever of 103 degrees F for about a day and a half total of 24-36 hour; This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (Had a 100 degrees F fever ongoing until today/in the morning he will have a fever of 99.1 ranging to 101 degrees F by evening), CHILLS (Chills when traveling on the plane), MYALGIA (Felt achy) and PYREXIA (Fever of 103 degrees F for about a day and a half total of 24-36 hour) in a 52-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 014F21A and 939902) for COVID-19 vaccination. Concomitant products included VALACICLOVIR HYDROCHLORIDE (VALTREX) for HSV infection. On 26-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 24-Sep-2021, the patient experienced MYALGIA (Felt achy) and PYREXIA (Fever of 103 degrees F for about a day and a half total of 24-36 hour). On 01-Oct-2021, the patient experienced PYREXIA (Had a 100 degrees F fever ongoing until today/in the morning he will have a fever of 99.1 ranging to 101 degrees F by evening) and CHILLS (Chills when traveling on the plane). The patient was treated with PARACETAMOL, PHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE (THERAFLU [PARACETAMOL;PHENIRAMINE MALEATE;PHENYLEPHRINE HYDROCHLORIDE]) for Adverse reaction, at a dose of 1 dosage form. On 25-Sep-2021, MYALGIA (Felt achy) and PYREXIA (Fever of 103 degrees F for about a day and a half total of 24-36 hour) had resolved. At the time of the report, PYREXIA (Had a 100 degrees F fever ongoing until today/in the morning he will have a fever of 99.1 ranging to 101 degrees F by evening) had not resolved and CHILLS (Chills when traveling on the plane) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 24-Sep-2021, Body temperature: 103 (High) 103 degrees F. On 01-Oct-2021, Body temperature: 100 (High) 100 degrees F. On 02-Oct-2021, SARS-CoV-2 test: negative (Negative) Negative. On an unknown date, Body temperature: 99.1 to 101 (High) Fever of 99.1 ranging to 101 degrees F. This case was linked to MOD-2021-344216 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: Fever of 99.1 ranging to 101 degrees F; Test Date: 20210924; Test Name: Body temperature; Result Unstructured Data: 103 degrees F; Test Date: 20211001; Test Name: Body temperature; Result Unstructured Data: 100 degrees F; Test Date: 20211002; Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- VALTREX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 26.08.2021
- Beginn
- 26.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
Painful left arm for 24 hours; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Painful left arm for 24 hours) in a 52-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. Concurrent medical conditions included Herpes simplex type I. Concomitant products included VALACICLOVIR HYDROCHLORIDE (VALTREX) for Herpes simplex type I. On 26-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Aug-2021, the patient experienced PAIN IN EXTREMITY (Painful left arm for 24 hours). On 27-Aug-2021, PAIN IN EXTREMITY (Painful left arm for 24 hours) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment medications were reported. This case was linked to MOD-2021-344229 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Herpes simplex type I
- Vorgeschichte
- -
- Andere Medikamente
- VALTREX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 11.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Influenza
Pain in extremity
Symptomtext
Felt a little flu-ey; arm was a little sore; This spontaneous case was reported by a consumer and describes the occurrence of INFLUENZA (Felt a little flu-ey) and PAIN IN EXTREMITY (arm was a little sore) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The patient's past medical history included COVID-19 (The patient put off having the vaccination because they felt they had antibodies.) in January 2021 and Hip surgery (Bad back.). Concomitant products included PARACETAMOL (TYLENOL), GABAPENTIN, TRAMADOL, IRON, OLMESARTAN, ATORVASTATIN, LORATADINE and MONTELUKAST for an unknown indication. On 11-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced INFLUENZA (Felt a little flu-ey) and PAIN IN EXTREMITY (arm was a little sore). At the time of the report, INFLUENZA (Felt a little flu-ey) and PAIN IN EXTREMITY (arm was a little sore) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The treatment information was unknown. This case was linked to MOD-2021-344232 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (The patient put off having the vaccination because they felt they had antibodies.); Hip surgery (Bad back.)
- Andere Medikamente
- TYLENOL; GABAPENTIN; TRAMADOL; IRON; OLMESARTAN; ATORVASTATIN; LORATADINE; MONTELUKAST
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 13.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Injection site pain
Injection site swelling
Symptomtext
Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anxiety
Crying
Headache
Symptomtext
Severe anxiety and uncontrollable crying. I also had a severe headache for a few days. These symptoms lasted for one week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Seasonal asthma when allergies are acting up.
- Andere Medikamente
- I am not on any prescription medications and take zinc, vitamin C and magnesium but did not take this 3 days prior to the vaccine or more than a week afterwards
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 09.10.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site bruising
Injection site haemorrhage
Injection site swelling
Needle issue
Symptomtext
Site: Bruising at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: The needle initially did not go in easily (only the point) so I changed the needle. During 2nd attempt, needle went in fine, I administerd the vaccine, upon removal of the syringe, there was slight bleeding and I used a cotton ball and it stopped bleeding. Afterwards I noticed swelling at the injection site the size of a nickle. Pt had no other reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 16.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: ja
Cataract operation
Chills
Extra dose administered
Malaise
Pain
Pyrexia
Symptomtext
Aches, chills, fever of 101. Generally felt terrible the entire day August 17th after 3rd Moderna shot on August 16th. Fever brought down by tylenol, but I hardly ever run a fever, so 101 was very high for me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- ER VISIT - Pressure in right eye was 55. ER doc consulted with Ophthalmologist. Ophthalmologist saw me immediately after leaving ER. Pressure was down to 35, but not out of danger. Ophthalmologist referred me to another doctor at a laser center. On Tuesday, August 24th, Dr. performed lazer procedure to bring down eye pressure in both eyes. On Sept 29th I had cataract surgery in right eye to prevent a recurrence. Left eye procedure repeated on Oct. 6th.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Common variable immunodeficiency (CVID) is an immune system disorder that causes you to have low levels of the proteins that help fight infections. If you have CVID , you'll likely have repeated infections in your ears, sinuses and respiratory system
- Andere Medikamente
- Wellbutrin Celexa Vitamin D-3 NP Thyroid
- Allergien
- Sulfa drugs Codine Shrimp
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 09.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse event
Injection site oedema
Injection site pain
Loss of personal independence in daily activities
Myalgia
Symptomtext
injection site edema and pain for + 2 weeks since injection. Unusual time frame for long term pain at site and localized muscle pain making it difficult to use arms for regular occupational activities required daily since that injection . This is an adverse event reaction for me since I have had COVID injections prior to this 2nd dosing and many other vaccines for polio, MMR, DTaP, pneumonia,etc.....
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site oedema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Hypersensitivity
Pruritus
Rash erythematous
Urticaria
Symptomtext
red bumps that itched and felt like they were burning; red bumps that itched and felt like they were burning; red bumps that itched and felt like they were burning; hives; allergic reaction spread throughout the torso, neck, behind the ears and down the arms; This spontaneous case was reported by a consumer and describes the occurrence of RASH ERYTHEMATOUS (red bumps that itched and felt like they were burning), PRURITUS (red bumps that itched and felt like they were burning), BURNING SENSATION (red bumps that itched and felt like they were burning), URTICARIA (hives) and HYPERSENSITIVITY (allergic reaction spread throughout the torso, neck, behind the ears and down the arms) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. Concurrent medical conditions included Nail infection and Sleep problem. Concomitant products included HYDROCHLOROTHIAZIDE for Blood pressure management, TERBINAFINE for Nail infection, GABAPENTIN for Sleep problem, ETANERCEPT (ENBREL) for an unknown indication. On 29-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Sep-2021, the patient experienced RASH ERYTHEMATOUS (red bumps that itched and felt like they were burning), PRURITUS (red bumps that itched and felt like they were burning), BURNING SENSATION (red bumps that itched and felt like they were burning), URTICARIA (hives) and HYPERSENSITIVITY (allergic reaction spread throughout the torso, neck, behind the ears and down the arms). The patient was treated with PREDNISONE for Hives, at an unspecified dose and frequency. At the time of the report, RASH ERYTHEMATOUS (red bumps that itched and felt like they were burning), PRURITUS (red bumps that itched and felt like they were burning), BURNING SENSATION (red bumps that itched and felt like they were burning), URTICARIA (hives) and HYPERSENSITIVITY (allergic reaction spread throughout the torso, neck, behind the ears and down the arms) had not resolved. Patient started getting red bumps that itched and felt like they were burning. This allergic reaction spread throughout the torso, neck, behind the ears and down the arms. Those symptoms are ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Nail infection; Sleep problem
- Vorgeschichte
- -
- Andere Medikamente
- HYDROCHLOROTHIAZIDE; TERBINAFINE; GABAPENTIN; ENBREL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- 17.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 12,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram head
Ear pain
Herpes zoster
Impaired work ability
Lipoma
Pain
Rash
Symptomtext
I got shingles within 2 weeks after my 2nd shot. No hx health problems. I believe it to be a severe case on my face. I spent time in the ER due to this and despite treatment, still in severe pain 1.5 weeks after the initial onset of sxs. I am unable to work due to the pain. This was 2 weeks after my 2nd Moderna shot. I also had a lipoma grow on my forearm within 2 weeks after my first shot. No hx of lipomas, and no family hx of them either. I now have to have it removed by a general surgeon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- CT of the head due to severe ear pain prior to the rash showing up. Will also be seeing a general surgeon in a couple of weeks to have a lipoma removed.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 10.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pruritus
Lymphadenopathy
Symptomtext
Large, red, itchy circle on right arm at injection site. Swollen lymph node in right armpit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Collagen, herbal tea
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Influenza like illness
Nausea
Photophobia
Pyrexia
Vaccination site urticaria
Vision blurred
Symptomtext
she noted huge hives (3-4 inches) which started at the injection site (left arm); fever; chills; was feeling "fluish"; nauseous; dizzy; vision smoky; light her my eye; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (dizzy), VISION BLURRED (vision smoky), PHOTOPHOBIA (light her my eye), INFLUENZA LIKE ILLNESS (was feeling "fluish") and NAUSEA (nauseous) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 10-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Aug-2021, the patient experienced DIZZINESS (dizzy), VISION BLURRED (vision smoky), PHOTOPHOBIA (light her my eye) and NAUSEA (nauseous). On 11-Aug-2021, the patient experienced INFLUENZA LIKE ILLNESS (was feeling "fluish"), PYREXIA (fever) and CHILLS (chills). On 16-Aug-2021, the patient experienced VACCINATION SITE URTICARIA (she noted huge hives (3-4 inches) which started at the injection site (left arm)). The patient was treated with PREDNISONE ACETATE (PREDNISONE [PREDNISONE ACETATE]) for Vaccination site urticaria, at an unspecified dose and frequency and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL ALLERGY [DIPHENHYDRAMINE HYDROCHLORIDE]) for Vaccination site urticaria, at an unspecified dose and frequency. On 10-Aug-2021, DIZZINESS (dizzy) and NAUSEA (nauseous) outcome was unknown, VISION BLURRED (vision smoky) and PHOTOPHOBIA (light her my eye) had resolved. On 13-Aug-2021, INFLUENZA LIKE ILLNESS (was feeling "fluish"), PYREXIA (fever) and CHILLS (chills) had resolved. On 18-Aug-2021, VACCINATION SITE URTICARIA (she noted huge hives (3-4 inches) which started at the injection site (left arm)) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 08.09.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Pain in extremity
Pyrexia
Symptomtext
arm hurt for a week; ran a slight fever; She thinks the vaccine was administered too high in her arm and may have hit her bone; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (arm hurt for a week), PYREXIA (ran a slight fever) and INCORRECT ROUTE OF PRODUCT ADMINISTRATION (She thinks the vaccine was administered too high in her arm and may have hit her bone) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The patient's past medical history included Unconscious (patient was found unconscious due to anemia from her bleeding colon.) and Parathyroid gland operation. Concurrent medical conditions included Bleeding colon ulcer, Osteoporosis and Anemia. Concomitant products included FENTANYL for Osteoporosis. On 08-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In September 2021, the patient experienced PAIN IN EXTREMITY (arm hurt for a week), PYREXIA (ran a slight fever) and INCORRECT ROUTE OF PRODUCT ADMINISTRATION (She thinks the vaccine was administered too high in her arm and may have hit her bone). In September 2021, INCORRECT ROUTE OF PRODUCT ADMINISTRATION (She thinks the vaccine was administered too high in her arm and may have hit her bone) had resolved. At the time of the report, PAIN IN EXTREMITY (arm hurt for a week) was resolving and PYREXIA (ran a slight fever) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. treatment to the events not reported. patient has a history of a bleeding colon and very sick ,can't go to the bathroom like a normal person. Patient has the bones of a 200-year-old woman after an operation on her parathyroid glands,and has bad osteoporosis. Patient had a recent event was found unconscious due to anemia from her bleeding colon. She was given 8 pints of blood following this event. Her gastroenterologist wants to perform an operation on her where they will remove a large part of her colon and hospitalize her for almost a month. Her doctor wanted her to get the COVID-19 vaccine prior to being hospitalized. Patient is not sure if the vaccine was given by intramuscular injection because she thinks it was administered wrong and thinks that vaccine was administered too high in her arm and may have hit her bone. Patient thought that after working with animals who had coronavirus her whole life. She thought she would have a natural immunity, but she does not.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Anemia; Bleeding colon ulcer; Osteoporosis
- Vorgeschichte
- Medical History/Concurrent Conditions: Parathyroid gland operation; Unconscious (patient was found unconscious due to anemia from her bleeding colon.)
- Andere Medikamente
- FENTANYL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 07.09.2021
- Beginn
- 07.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Fatigue
Hypoaesthesia
Loss of personal independence in daily activities
Muscle spasms
Sleep disorder
Symptomtext
Fatigue started at 8pm and was sudden onset, but felt like I couldn't move. Extreme exhaustion remained through the night and an additional 2 days. Activities of daily living were very difficult. I developed numbness in my arms(from elbows to hands) that still persists today. I also suffered from cramping in my lower legs, preventing me from sleeping or getting comfortable. The cramping turned to muscle spasms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Ulcerative colitis, fibromyalgia, migraines
- Andere Medikamente
- Xeljanz, NP thyroid, L-Thyroxine, Prometrium, spironolactone, sumitriptan, ubrelvey, magnesium, fiber(methylcellulose), Lipitor Vitamin D3, Zinc
- Allergien
- Iodine dye, percocet
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 21.08.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blepharospasm
Headache
Joint stiffness
Tinnitus
Symptomtext
Constant humming in Left ear that has not stopped like tinnitus (MD appointment pending ) , headache - constant, joint stiffness in neck, Left eye twitching several times / day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none yet, MD asked me to wait and see if symptoms persist
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- phentermine 18.75 mg daily
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
I have hives all over my back, chest stomach, neck, behind ears, lower abdomen, underarms, shoulder, and itchy ears
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- Enbrel, terbinafine, gabapentin, hydrochlotothiazide
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 13.09.2021
- Beginn
- 13.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cellulitis
Chills
Dizziness
Erythema
Gait disturbance
Headache
Hypersensitivity
Pain
Pain in extremity
Peripheral swelling
Sensation of foreign body
Tenderness
Vertigo
Symptomtext
within the first hour dizziness, headache, feeling like something was stock in throat when trying to eat. progressed to all over body pain, aches, chills then severe pain in right arm. arm began swelling to double size. Then it became red and painful to the touch. Patient was seen in clinic and diagnosed with delayed hypersensitivity reaction and given steroid and benadryl and oral antibiotic c was also given for cellulitis and shot of rocephin. Then a few days later developed severe vertigo and difficulty walking. Patient was given oral medications for vertigo but they are ineffective .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Migraines, acid reflux
- Vorgeschichte
- none
- Andere Medikamente
- protonix, topamax
- Allergien
- sulfa, morphine sulfate, iodine, shellfish
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 01.10.2021
- Impfdatum
- 25.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dry skin
Pruritus
Swelling
Vaccination site pain
Vaccination site pruritus
Vaccination site urticaria
Symptomtext
skin is very scabby; it's spreading on entire left side of the body/leg is itching/back is itching/itching is on the inside of flesh; bad hives; swelling; little itchy/super duper itchy/scratched my arm to the point of bleeding; the day of injection my arm was really sore; This spontaneous case was reported by a consumer and describes the occurrence of SWELLING (swelling), DRY SKIN (skin is very scabby), PRURITUS (it's spreading on entire left side of the body/leg is itching/back is itching/itching is on the inside of flesh), VACCINATION SITE PRURITUS (little itchy/super duper itchy/scratched my arm to the point of bleeding) and VACCINATION SITE PAIN (the day of injection my arm was really sore) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 25-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-Aug-2021, the patient experienced SWELLING (swelling), VACCINATION SITE PRURITUS (little itchy/super duper itchy/scratched my arm to the point of bleeding) and VACCINATION SITE PAIN (the day of injection my arm was really sore). On 28-Aug-2021, the patient experienced DRY SKIN (skin is very scabby), PRURITUS (it's spreading on entire left side of the body/leg is itching/back is itching/itching is on the inside of flesh) and VACCINATION SITE URTICARIA (bad hives). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Adverse event, at an unspecified dose and frequency. On 28-Aug-2021, VACCINATION SITE PAIN (the day of injection my arm was really sore) had resolved. At the time of the report, SWELLING (swelling) was resolving, DRY SKIN (skin is very scabby), PRURITUS (it's spreading on entire left side of the body/leg is itching/back is itching/itching is on the inside of flesh) and VACCINATION SITE URTICARIA (bad hives) outcome was unknown and VACCINATION SITE PRURITUS (little itchy/super duper itchy/scratched my arm to the point of bleeding) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant drug details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 17.08.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 29,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Balance disorder
Chills
Illness
Pyrexia
SARS-CoV-2 test
Symptomtext
she got sick; she could not keep her balance; high fever; chills; her joints hurt; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (she got sick), BALANCE DISORDER (she could not keep her balance), PYREXIA (high fever), CHILLS (chills) and ARTHRALGIA (her joints hurt) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 939902 and 048F21A) for COVID-19 vaccination. Concomitant products included AMITRIPTYLINE, ATORVASTATIN, CYCLOBENZAPRINE, GABAPENTIN, HYDROCHLOROTHIAZIDE, POTASSIUM CHLORIDE (KLOR-CON), LEVOTHYROXINE, LISINOPRIL, MELOXICAM, METOPROLOL, PANTOPRAZOLE, PAROXETINE and FLUTICASONE FUROATE, UMECLIDINIUM BROMIDE, VILANTEROL TRIFENATATE (TRELEGY) for an unknown indication. On 17-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 15-Sep-2021, the patient experienced ILLNESS (she got sick) (seriousness criterion medically significant), BALANCE DISORDER (she could not keep her balance) (seriousness criterion medically significant), PYREXIA (high fever) (seriousness criterion medically significant), CHILLS (chills) (seriousness criterion medically significant) and ARTHRALGIA (her joints hurt) (seriousness criterion medically significant). At the time of the report, ILLNESS (she got sick), BALANCE DISORDER (she could not keep her balance), PYREXIA (high fever), CHILLS (chills) and ARTHRALGIA (her joints hurt) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, SARS-CoV-2 test: negative (Negative) Negative. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Treatment information was not provided. Company comment: This case concerns a 68-year-old, female patient with no relevant medical history, who experienced the unexpected events of Illness, balance disorder and expected events of Pyrexia, Chills and Arthralgia. The events occurred 29 days after the second dose of Moderna Covid-19 vaccine. The rechallenge was not applicable, as the events did not happened after the first dose. The events were considered related to the product per the reporter's assessment. The events of Pyrexia, Chills and Arthralgia are consistent with the current understanding of the mechanism of action of the study medication The benefit-risk relationship of Moderna Covid-19 vaccine is not affected by this report.; Sender's Comments: This case concerns a 68-year-old, female patient with no relevant medical history, who experienced the unexpected events of Illness, balance disorder and expected events of Pyrexia, Chills and Arthralgia. The events occurred 29 days after the second dose of Moderna Covid-19 vaccine. The rechallenge was not applicable, as the events did not happened after the first dose. The events were considered related to the product per the reporter's assessment. The events of Pyrexia, Chills and Arthralgia are consistent with the current understanding of the mechanism of action of the study medication The benefit-risk relationship of Moderna Covid-19 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- AMITRIPTYLINE; ATORVASTATIN; CYCLOBENZAPRINE; GABAPENTIN; HYDROCHLOROTHIAZIDE; KLOR-CON; LEVOTHYROXINE; LISINOPRIL; MELOXICAM; METOPROLOL; PANTOPRAZOLE; PAROXETINE; TRELEGY
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 28.09.2021
- Impfdatum
- 25.08.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Mechanical urticaria
Rash
Urticaria
Symptomtext
24 hours after receiving the vaccine I had chills and diarrhea which seemed standard. However, a week after the injection, the diarrhea came back for 48 hours and I broke out in full body hives. Since the initial breakout, I have hives that come and go which I treat with an OTC anti-histamine and I have dermatographia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Armour Thyroid and Gianvi
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 28.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Breakthrough COVID case after vaccination, had subjective fever and chills onset 9/27/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID Antigen positive on 9/28/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- cardiovascular disease, chronic lung problems
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 04.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 17,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Headache
Menstruation delayed
Muscle spasms
Symptomtext
Missed period. I had terrible cramps and headaches about a week after the vaccine but never had my monthly cycle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Prenatal, Vitamin D3, Vitamin C, Probiotic, Vitamin E, P5P, B complex, Collagen, Levothyroxin 75 MCG, Metformin 1000, Cabergoline .25 mg
- Allergien
- None known.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Laboratory test
Rash erythematous
Rash pruritic
Symptomtext
Red itchy rash covering most of my torso. The rash had fluid filled pustule's and continued to develop to the extremities over the next several days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- Nurse practitioner took a swab of several pustules and reportedly sent them to a lab to be analyzed.
- Aktuelle Erkrankungen
- Hives subsequent to 1st vaccine
- Vorgeschichte
- -
- Andere Medikamente
- Do not have a listing of medicines currently taking
- Allergien
- None
- Vorherige Impfungen
- After first vaccine, got a bad case of hives
- Staat
- AR
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 24.09.2021
- Impfdatum
- 09.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 14,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site rash
Rash
Rash erythematous
Symptomtext
Red painful rash around the injection site that lasted approximately 2 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 15.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash erythematous
Rash pruritic
Swelling
Symptomtext
Covid arm - large red rash, 4 to 5 quarters in size, itchy, large bump
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal vitamin & currently breastfeeding. Had a mole removal minor surgery (local injectable numbing agent) the day before adverse reaction
- Allergien
- Macrobid - developed rash
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Feeling abnormal
Head discomfort
Myalgia
Vaccination complication
Symptomtext
Feeling terrible; Can not even hold head up; I get up and eat then go back to bed"; Muscle pain; Joint pain; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (Feeling terrible), HEAD DISCOMFORT (Can not even hold head up), VACCINATION COMPLICATION (I get up and eat then go back to bed"), MYALGIA (Muscle pain) and ARTHRALGIA (Joint pain) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 02-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Sep-2021, the patient experienced FEELING ABNORMAL (Feeling terrible), HEAD DISCOMFORT (Can not even hold head up), VACCINATION COMPLICATION (I get up and eat then go back to bed"), MYALGIA (Muscle pain) and ARTHRALGIA (Joint pain). At the time of the report, FEELING ABNORMAL (Feeling terrible), HEAD DISCOMFORT (Can not even hold head up), VACCINATION COMPLICATION (I get up and eat then go back to bed"), MYALGIA (Muscle pain) and ARTHRALGIA (Joint pain) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No Concomitant medications were provided No treatment medications were provided. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 22.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Erythema
Pruritus
Rash
Skin swelling
Urticaria
Symptomtext
They are puffy/They swell like welts; She has bruised her body from scratching,she can't help it; They start as red dots; Extremely itchy/ they itch so bad; They swell like welts; A rash in the inner side of her left forearm and is now all over the body / started in the left arm and then went to the right arm, ankles, legs, waist, hip area, stomach and side of the breasts; This spontaneous case was reported by a consumer and describes the occurrence of SKIN SWELLING (They are puffy/They swell like welts), CONTUSION (She has bruised her body from scratching,she can't help it), ERYTHEMA (They start as red dots), PRURITUS (Extremely itchy/ they itch so bad) and URTICARIA (They swell like welts) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 22-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In August 2021, the patient experienced SKIN SWELLING (They are puffy/They swell like welts), CONTUSION (She has bruised her body from scratching,she can't help it), ERYTHEMA (They start as red dots), PRURITUS (Extremely itchy/ they itch so bad), URTICARIA (They swell like welts) and RASH (A rash in the inner side of her left forearm and is now all over the body / started in the left arm and then went to the right arm, ankles, legs, waist, hip area, stomach and side of the breasts). The patient was treated with METHYLPREDNISOLONE (MEDROL DOSEPAK) for Adverse event, at an unspecified dose and frequency. At the time of the report, SKIN SWELLING (They are puffy/They swell like welts), CONTUSION (She has bruised her body from scratching,she can't help it), ERYTHEMA (They start as red dots), PRURITUS (Extremely itchy/ they itch so bad), URTICARIA (They swell like welts) and RASH (A rash in the inner side of her left forearm and is now all over the body / started in the left arm and then went to the right arm, ankles, legs, waist, hip area, stomach and side of the breasts) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient reported that she is on some medications. It was reported that patient experienced adverse events 7 days post her first dose and thought the adverse events occurred was due to poison ivy.The patient is unsure about getting her second dose. She had an appointment with her rheumatologist on 14-Sep-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Diarrhoea
Headache
Myalgia
Oropharyngeal pain
Pyrexia
Symptomtext
Fever, sore throat, cough, headache, diarrhea, muscle pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 25.08.2021
- Beginn
- 26.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Pruritus
Rash
Symptomtext
Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash Generalized-Medium, Additional Details: Patient called on 9/21/21 regarding long term hives and itching after vaccine. Patient was advised to take a benadryl to help with hives and itching (she has not done so due to concer that it might affect the efficacy). patient cancelled appointment for second dose until resolution of symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 25.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Injection site urticaria
Rash pruritic
Symptomtext
Pt. states that after receiving the 1st dose of Moderna 08/25/2021, started experiencing symptoms 09/01/2021 of an itchy rash developing in and around the injection site. Entire left side of injection site covered in hives. No Primary visit noted. Still continuing to experience symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Clam
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site mass
Pain in extremity
Skin warm
Symptomtext
-Arm soreness started a couple of hours after injection and lasted for about 1 week -warm to touch: started around 10 hours after injection and lasted about 24 hours total - small knot/lump around injection site: started about 12 hours after injection and lasted about 24 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site mass
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- -
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 21.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Myalgia
Pyrexia
Symptomtext
he is complaining of lots of muscle pain/the muscle ache is moderate/muscle ache is still ongoing; he had high fevers as well/his fever was 103F; This spontaneous case was reported by a nurse and describes the occurrence of MYALGIA (he is complaining of lots of muscle pain/the muscle ache is moderate/muscle ache is still ongoing) and PYREXIA (he had high fevers as well/his fever was 103F) in a 48-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The patient's past medical history included COVID-19 in 2020 and Mechanical ventilation in 2020. On 02-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Sep-2021, the patient experienced MYALGIA (he is complaining of lots of muscle pain/the muscle ache is moderate/muscle ache is still ongoing) and PYREXIA (he had high fevers as well/his fever was 103F). The patient was treated with IBUPROFEN (MOTRIN [IBUPROFEN]) for Fever, at an unspecified dose and frequency and METHOCARBAMOL (ROBAXIN) for Adverse event, at an unspecified dose and frequency. On 03-Sep-2021, PYREXIA (he had high fevers as well/his fever was 103F) had resolved. At the time of the report, MYALGIA (he is complaining of lots of muscle pain/the muscle ache is moderate/muscle ache is still ongoing) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In September 2021, Body temperature: 103 (High) 103 F. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication provided by the reporter It was reported that the patient was a healthy person with no comorbidities and he exercise regularly He had infected with COVID 19 and nearly lost his life as he was on ventilator His wife reported that he had a natural immunity against the virus Most recent FOLLOW-UP information incorporated above includes: On 09-Sep-2021: Follow-up contains lot number updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- Test Date: 202109; Test Name: Body temperature; Result Unstructured Data: 103 F
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19; Mechanical ventilation
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 20.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blister
Blood urine present
Epistaxis
Erythema
Gingival bleeding
Swelling
Urticaria
Symptomtext
Patient reported hives, swelling, redness and blisters on feet. Her foot was completely red and covered in blisters. Nose bleeds and bleeding gums and blood in the urine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- none reported
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Ciprofloxacin and Penicillin
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 19.09.2021
- Impfdatum
- 15.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Decreased appetite
Fatigue
Headache
Hot flush
Influenza like illness
Nausea
Pain
Pyrexia
Symptomtext
Symptoms began at approximately 3:00AM on 09/16/2021, 18 hours after the vaccine was administered: Flu like symptoms-fever of 100.7, chills, hot flashes, body aches, fatigue, headache. All lasting approximately 24 hours. Treated with acetaminophen 500mg for fever and pain every 4 hours. Fatigue, loss of appetite, and intermittent nausea lasting for an additional 72 hours. No treatment given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression, obesity
- Andere Medikamente
- Celexa, 40mg daily Saxenda 0.6 mg daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 18.09.2021
- Impfdatum
- 14.09.2021
- Beginn
- 14.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives. One hive on day 1 then covered in hives from head to toes and still not resolved at time of filing report
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anxiety
- Andere Medikamente
- Venlafaxine Semaglitude
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 05.09.2021
- Beginn
- 05.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Hyperhidrosis
Myalgia
Nausea
Pyrexia
Symptomtext
Fever, severe muscle aches, chills, sweats, nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Adderall 20mg bid, multi vitamin, vitamin c, b-12 complex, vitamin d, biotin, baby aspirin
- Allergien
- Anaphylactic pine nut allergy
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 08.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Symptomtext
Mild general pain / pain in the body; Pain in the arm; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Mild general pain / pain in the body) and PAIN IN EXTREMITY (Pain in the arm) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 08-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced PAIN (Mild general pain / pain in the body) and PAIN IN EXTREMITY (Pain in the arm). At the time of the report, PAIN (Mild general pain / pain in the body) and PAIN IN EXTREMITY (Pain in the arm) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. No concomitant medications reported. No treatment information was reported by reporter. This case was linked to MOD-2021-313125 (Patient Link). Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 01.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Vaccination site movement impairment
Vaccination site pain
Symptomtext
Arm doubled in size\ Expansion of the inflammation to the lower arm; Loss of mobility in the arm; Sore arm/ pain in the arm; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE MOVEMENT IMPAIRMENT (Loss of mobility in the arm), VACCINATION SITE PAIN (Sore arm/ pain in the arm) and VACCINATION SITE SWELLING (Arm doubled in size\ Expansion of the inflammation to the lower arm) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 01-Sep-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 02-Sep-2021, the patient experienced VACCINATION SITE MOVEMENT IMPAIRMENT (Loss of mobility in the arm), VACCINATION SITE PAIN (Sore arm/ pain in the arm) and VACCINATION SITE SWELLING (Arm doubled in size\ Expansion of the inflammation to the lower arm). At the time of the report, VACCINATION SITE MOVEMENT IMPAIRMENT (Loss of mobility in the arm), VACCINATION SITE PAIN (Sore arm/ pain in the arm) and VACCINATION SITE SWELLING (Arm doubled in size\ Expansion of the inflammation to the lower arm) outcome was unknown. Concomitant drug was not reported. Treatment medication was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 17.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Head discomfort
Lymphadenopathy
Myalgia
Neck pain
Spinal pain
Symptomtext
Lymph node swelling on both sides of her neck; Really bad muscle aches; sore at the top of her neck/sore around spinal cord area on her neck; The pain went to the base of her skull around the spinal cord; burning sensation; Her head felt heavy; The pain went to the back of her neck; This spontaneous case was reported by a consumer and describes the occurrence of LYMPHADENOPATHY (Lymph node swelling on both sides of her neck), MYALGIA (Really bad muscle aches), NECK PAIN (sore at the top of her neck/sore around spinal cord area on her neck), SPINAL PAIN (The pain went to the base of her skull around the spinal cord) and BURNING SENSATION (burning sensation) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 17-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced LYMPHADENOPATHY (Lymph node swelling on both sides of her neck), MYALGIA (Really bad muscle aches), NECK PAIN (sore at the top of her neck/sore around spinal cord area on her neck), SPINAL PAIN (The pain went to the base of her skull around the spinal cord), BURNING SENSATION (burning sensation), HEAD DISCOMFORT (Her head felt heavy) and NECK PAIN (The pain went to the back of her neck). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) ongoing since an unknown date at an unspecified dose and frequency. At the time of the report, LYMPHADENOPATHY (Lymph node swelling on both sides of her neck), MYALGIA (Really bad muscle aches), SPINAL PAIN (The pain went to the base of her skull around the spinal cord), BURNING SENSATION (burning sensation), HEAD DISCOMFORT (Her head felt heavy) and NECK PAIN (The pain went to the back of her neck) outcome was unknown and NECK PAIN (sore at the top of her neck/sore around spinal cord area on her neck) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient had taken 6 days of steroids and antibiotics for head and neck effects No concomitant medications were provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 04.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Symptomtext
Site: Redness at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 08.09.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Ear pain
Fatigue
Flushing
Headache
Hyperhidrosis
Illness
Injection site pain
Injection site swelling
Nausea
Pain
Pyrexia
Vomiting
Symptomtext
Site: Swelling at Injection Site-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, Systemic: Fever-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Headache-Severe, Systemic: Vomiting-Severe, Additional Details: Patient was out severly sick for 5 days. Experienced severe fatigue, nausea,vomiting, headache, fever and pain at injection site. Arm that it was given in was swollen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 16.09.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Fatigue
Pain
Pyrexia
Symptomtext
I received a third dose of the Moderna COVID-19 vaccine per the advice of my physician, as I am immunosuppressed. (My first and second doses were in March and April of this year.) Within 24 hours of receiving my third dose of the vaccine, I was in bed with a 103 fever, fatigue, chills, and body aches that lasted 18-20 hours. After my fever broke, my temperature was 95 and I had fatigue, chills and body aches for the next 12 to 15 hours. All of the symptoms went away after about three days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None-smoker non-drinker
- Vorgeschichte
- Rheumatoid arthritis, POTS, chronic migraine
- Andere Medikamente
- Enbrel Sulfasalzine Evoxac Atenolol Duloxetine Lo loesterin Zyrtec Dymista Restatis Flowvent Omeprazole Vypeti Multivitamin, Vitamin C, Vitamin D, Sudafed, Mucinex, Excedrin, Probiotics
- Allergien
- Airborne allergies only - mold, pollen, dust, etc.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 16.09.2021
- Impfdatum
- 23.08.2021
- Beginn
- 24.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest X-ray
Chills
Electrocardiogram
Headache
Pain
Pyrexia
Symptomtext
08/24/2021 around midnight woke up with high fever, headache, chills and body aches. The fever ended after about 24 hours, the headache and body aches lasted for three days. Still having a lingering pain on the right side below shoulder area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Unknown date-just about a week after the onset of symptoms EKG-normal Chest x-ray-normal
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- allergies
- Andere Medikamente
- I take Metformin, Rosatatin,
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 15.09.2021
- Impfdatum
- 21.08.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fatigue
Feeling hot
Laboratory test normal
Photophobia
Pruritus
Pyrexia
Rash
Symptomtext
08/22/2021 I was very fatigued, felt feverish and hot, I got a rash and itchy. light hurt my eyes. I still get the rash every night about the same time night at 11pm and still on going. 09/06/2021 I went to urgent care, I am taking Zyrtec.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 09/06/2021 did lab work-all was normal
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 15.09.2021
- Impfdatum
- 17.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Vertigo
Symptomtext
Vertigo onset 12 hours after administration, light headed feeling persists 4 weeks later, treated with light dose of meclizine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Non Hodgkin lymphoma
- Andere Medikamente
- 1/2 mg Haldol, sr multivitamin, 25mcg Vitamin D3, 500 mg lysine
- Allergien
- Lomotil, simvistatin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 14.09.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Product administered to patient of inappropriate age
Symptomtext
Patient is under 18 y.o and was administered moderna vaccine. Patient reports sore arm with first dose, no other compliants.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 07.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Feeling abnormal
Illness
Mouth ulceration
Myalgia
Pyrexia
Vaccination site pain
Vaccination site swelling
Symptomtext
Chills; Injection site was pretty big; (Injection site) hurt really bad; Made her very sick; Feel really bad/ it was like having covid all over again; Had body aches; Had 100.1 F/ Fever; Ulcers inside my mouth; Very tired; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (Made her very sick), FEELING ABNORMAL (Feel really bad/ it was like having covid all over again), MOUTH ULCERATION (Ulcers inside my mouth), MYALGIA (Had body aches) and PYREXIA (Had 100.1 F/ Fever) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 in April 2021. On 07-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 07-Aug-2021, the patient experienced ILLNESS (Made her very sick), FEELING ABNORMAL (Feel really bad/ it was like having covid all over again), MYALGIA (Had body aches) and PYREXIA (Had 100.1 F/ Fever). On an unknown date, the patient experienced MOUTH ULCERATION (Ulcers inside my mouth), CHILLS (Chills), VACCINATION SITE SWELLING (Injection site was pretty big), VACCINATION SITE PAIN ((Injection site) hurt really bad) and FATIGUE (Very tired). The patient was treated with IBUPROFEN (MOTRIN [IBUPROFEN]) at an unspecified dose and frequency. At the time of the report, ILLNESS (Made her very sick), FEELING ABNORMAL (Feel really bad/ it was like having covid all over again), MOUTH ULCERATION (Ulcers inside my mouth), MYALGIA (Had body aches), PYREXIA (Had 100.1 F/ Fever), CHILLS (Chills), VACCINATION SITE SWELLING (Injection site was pretty big), VACCINATION SITE PAIN ((Injection site) hurt really bad) and FATIGUE (Very tired) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were mentioned. Patient stated that Second shot scheduled for 04Sep2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 29.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Diarrhoea
Faeces discoloured
Fatigue
Symptomtext
lower back aches that ache more than the rest of their body; Has had two episodes of loose bright orange stools; two episodes of loose bright orange stools; Tiredness; This spontaneous case was reported by a consumer and describes the occurrence of BACK PAIN (lower back aches that ache more than the rest of their body), DIARRHOEA (Has had two episodes of loose bright orange stools), FAECES DISCOLOURED (two episodes of loose bright orange stools) and FATIGUE (Tiredness) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 29-Aug-2021 at 2:00 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Aug-2021, the patient experienced BACK PAIN (lower back aches that ache more than the rest of their body), DIARRHOEA (Has had two episodes of loose bright orange stools), FAECES DISCOLOURED (two episodes of loose bright orange stools) and FATIGUE (Tiredness). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at a dose of 1 dosage form. At the time of the report, BACK PAIN (lower back aches that ache more than the rest of their body), DIARRHOEA (Has had two episodes of loose bright orange stools), FAECES DISCOLOURED (two episodes of loose bright orange stools) and FATIGUE (Tiredness) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Feeling abnormal
Hyperhidrosis
Peripheral swelling
Pyrexia
SARS-CoV-2 test negative
Secretion discharge
Vomiting
Symptomtext
On the first day around 4:00pm my arm swelled up all to my shoulder, under my arm, into my back and chest. I called the clinic where I received my vaccine and they said it was normal and to put ice on. I did put ice on it and it did not help. I went to bed and woke up around 6am with a fever around 102 and I was soaking wet from sweating. I began throwing up and had green snot. I felt horrible all over. About 9am I called minute clinic again and told them what was going on and they said it was normal to take Tylenol, drink fluids, and rest. Day 3 and day 4 no improvement and called minute clinic again and they said its normal and to wait. Day 5 I went to care now because minute clinic would not help me. They gave me an Augmentin and methylprednisolone. The doctor there said it was an obvious allergic reaction. I now think I have thrush from taking the steroids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Covid Test- neg.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- COPD
- Andere Medikamente
- Clairton D OTC, Singular 10mg, Albuterol inhaler AM/PM, Buspirone inhalation suspension 1mg, Flonase 50mg,
- Allergien
- sulfa, peanuts
- Vorherige Impfungen
- pneumonia about 5 years ago
- Staat
- OK
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 13.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Decreased appetite
Headache
Lethargy
Nausea
Neck pain
Pain
Pain in extremity
Symptomtext
Sore arm, shoulder & neck Headache Chills difficulty breathing deeply lethargic hurt all over nauseous didn't feel like eating conditions started to subside about 9:00 pm 9-11-2021. Almost gone 11:30 am on 9-13-2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Heart medications
- Andere Medikamente
- Clopidogrel Rosuvastatin Fenofibrate Losartin Ecotrin Levocitrizine Montelukast Pantoprazole Famotidine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 12.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Gingival discomfort
Gingival erythema
Gingival pain
Pain
Rash
Rash pruritic
Urticaria
Symptomtext
Left arm welts red all the way down to elbow, bumps on left and right arm, pain and rash that itches on left hand, left side of gums are really red and raw like a later peeled off very painful and burning. Fatigue, body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Rheumatoid arthritis, polyarthritis, fibromyalgia, neurothapy, mitral valve prolapse, asthma, anemia, vit d def, deaf in right ear, tremors, chronic fatigue syndrome
- Andere Medikamente
- Cymbalta 60mg bid Omeprazole 40mg daily
- Allergien
- Amoxicillin penicillin azithromycin Zyrtec cclore ketek zpak coreg gentamicin vancomycin omnicef, rocephin, imitrex, amitriptyline, cymbalta,
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 12.09.2021
- Impfdatum
- 31.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphasia
Feeling abnormal
Pain
Speech disorder
Symptomtext
Debilitating body pain starting roughly 24hours after 2nd dose of moderna shot. This all over pain subsided 16 hours after onset. Currently experiening ongoing symptoms of aphasia, brain fog. Word substitutions are becoming more frequent such as saying slide vs swing or colors wanting to say black but saying pink in addition to forgetting names of common items, and frequent use of talking around words I want to say example a definition or alternative word due to word searching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Xulane Birth Control
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 09.09.2021
- Impfdatum
- 31.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Keloid scar
Myalgia
Pyrexia
Symptomtext
Fever, chills, muscle aches, lethargy. Symptoms would come and go, were not continuous. Lasting 8 days. Took ibuprofen and rested. This was my third (booster) shot. First two shots did not have adverse symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, COPD, obesity
- Andere Medikamente
- Xanax, Albuterol, Amlodipine, Trelegy, Arnuity, Losartan, Fluticasone, Escitalopram, Montelukast, Multi-Vitamin, Calcium, Vitamin D, Milk Thistle, Vitamin B Complex, Fish Oil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 09.09.2021
- Impfdatum
- 08.09.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Pain
Symptomtext
chills throughout night, exhaustion, body aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 08.09.2021
- Impfdatum
- 28.08.2021
- Beginn
- 29.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pain in extremity
Symptomtext
Severe pain in left foot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 15.08.2021
- Beginn
- 26.08.2021
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Myalgia
Vaccination site erythema
Vaccination site nodule
Vaccination site swelling
Symptomtext
Fatigue; Sore arm; knot at the injection site.; red knot at the injection site.; swollen at the injection site.; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE NODULE (knot at the injection site.), VACCINATION SITE ERYTHEMA (red knot at the injection site.), VACCINATION SITE SWELLING (swollen at the injection site.), FATIGUE (Fatigue) and MYALGIA (Sore arm) in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History was provided. Concomitant products included ETONOGESTREL (NEXPLANON) for an unknown indication. On 15-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Aug-2021, the patient experienced VACCINATION SITE NODULE (knot at the injection site.), VACCINATION SITE ERYTHEMA (red knot at the injection site.) and VACCINATION SITE SWELLING (swollen at the injection site.). On an unknown date, the patient experienced FATIGUE (Fatigue) and MYALGIA (Sore arm). At the time of the report, VACCINATION SITE NODULE (knot at the injection site.), VACCINATION SITE ERYTHEMA (red knot at the injection site.), VACCINATION SITE SWELLING (swollen at the injection site.), FATIGUE (Fatigue) and MYALGIA (Sore arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Birth control orally and now injectable (Nexplanon) No Treatment Medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No Medical History was provided.
- Andere Medikamente
- NEXPLANON
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 05.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
Patient had sever itching and hives all over arms and back and body. It started the day after the vaccine. She took benadryl to help and it upset her stomach. The rash calmed but was not gone. She continued with symptoms until her next appointment. She stopped by pharmacy on 9/2 to get vaccine. We advised against it. She began Allegra and that has controlled symptoms since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- NKA
- Vorgeschichte
- NKA
- Andere Medikamente
- Patient took otc Benadryl once but experienced upset stomach the day after the vaccine. She continued with rashes. She came to pharmacy to explain on 9/2 and began Allegra to manage itching and had been taking daily since. it has helped
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 07.09.2021
- Impfdatum
- 14.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Vaccination site mass
Symptomtext
he had a bump that was about size of a golf ball,It went away completely after about 3 days. Now 4 days later, it came back. It's not as hard as before. The bump is at the injection site; He had a left sore arm.; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (He had a left sore arm.) and VACCINATION SITE MASS (he had a bump that was about size of a golf ball,It went away completely after about 3 days. Now 4 days later, it came back. It's not as hard as before. The bump is at the injection site) in a 35-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 14-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Aug-2021, the patient experienced PAIN IN EXTREMITY (He had a left sore arm.). On 15-Aug-2021, the patient experienced VACCINATION SITE MASS (he had a bump that was about size of a golf ball,It went away completely after about 3 days. Now 4 days later, it came back. It's not as hard as before. The bump is at the injection site). At the time of the report, PAIN IN EXTREMITY (He had a left sore arm.) outcome was unknown and VACCINATION SITE MASS (he had a bump that was about size of a golf ball,It went away completely after about 3 days. Now 4 days later, it came back. It's not as hard as before. The bump is at the injection site) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication details were provided. No treatment information was mentioned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 06.09.2021
- Impfdatum
- 04.09.2021
- Beginn
- 05.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Influenza like illness
Malaise
Myalgia
Pyrexia
Symptomtext
Flu like symptoms- fever, headache, muscle aches, fatigue, general malaise
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Herniated discs, depression, knee arthritis
- Andere Medikamente
- Desvenlafaxine Bariatric supplement Iron tablets Tylenol PM Cyclobenzaprine Prazosin Probiotic Omeprazole
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 05.09.2021
- Impfdatum
- 20.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Decreased appetite
Fatigue
Influenza like illness
Nausea
Pain
Tenderness
Vomiting
Symptomtext
The first weekend - flu-like aches and pains along with fatigue. (had lab work for an upcoming unrelated doctor's appointment and found out that numbers elevated indicating inflammation). The second weekend - Friday, August 27, became nauseous, throwing up around 7pm, reduced appetite the next 2 days, tender stomach, weak, fatigued, by Monday, August 30 - continued weak & fatigued, nausea mostly gone, appetite had returned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hoshimoto's Disease
- Andere Medikamente
- Nature-Throid, Bupropion, Montelukast, Progesterone pill, blend cream of estrogen/testosterone/progesterone, weekly allergy shots (not taken within a week of the booster vaccine shot), Supplements: Adapten, Nuadapt, cortisol manager, osteop
- Allergien
- latex
- Vorherige Impfungen
- mildly achey for a day or two
- Staat
- UT
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 27.08.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pruritus
Swelling
Symptomtext
Itchy, Swollen, hurting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 28.08.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site induration
Injection site nodule
Injection site swelling
Pruritus
Rash erythematous
Skin warm
Symptomtext
Covid arm Hard, swollen knots at injection site and below. Red rash Itch Pain Warm to touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site induration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Probiotic Vitamin C Vitamin D
- Allergien
- Lobster Crab
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 21.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Vaccination site erythema
Vaccination site pain
Vaccination site pruritus
Vaccination site swelling
Vaccination site warmth
Symptomtext
Injection site reaction; First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt; First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt; First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt; First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt; First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt.; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE REACTION (Injection site reaction), VACCINATION SITE WARMTH (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt), VACCINATION SITE PRURITUS (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt), VACCINATION SITE SWELLING (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt) and VACCINATION SITE ERYTHEMA (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included TELMISARTAN, ROSUVASTATIN CALCIUM (CRESTOR), LORATADINE and PREDNISONE for an unknown indication. On 21-Aug-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Aug-2021, the patient experienced INJECTION SITE REACTION (Injection site reaction), VACCINATION SITE WARMTH (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt), VACCINATION SITE PRURITUS (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt), VACCINATION SITE SWELLING (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt), VACCINATION SITE ERYTHEMA (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt) and VACCINATION SITE PAIN (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt.). At the time of the report, INJECTION SITE REACTION (Injection site reaction), VACCINATION SITE WARMTH (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt), VACCINATION SITE PRURITUS (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt), VACCINATION SITE SWELLING (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt), VACCINATION SITE ERYTHEMA (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt) and VACCINATION SITE PAIN (First it was itching, then 6 inches in diameter was hot, swollen and red. Also hurt.) outcome was unknown. The concomitant medication included benadryl.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- TELMISARTAN; CRESTOR; LORATADINE; PREDNISONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling hot
Rash
Vaccination site pain
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of FEELING HOT (warm to the touch), RASH (Rash on her left arm) and VACCINATION SITE PAIN (Left arm was sore) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Aug-2021, the patient experienced FEELING HOT (warm to the touch), RASH (Rash on her left arm) and VACCINATION SITE PAIN (Left arm was sore). At the time of the report, FEELING HOT (warm to the touch), RASH (Rash on her left arm) and VACCINATION SITE PAIN (Left arm was sore) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No Concomitant Medications were provided. No Treatment Medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Rash pruritic
Skin reaction
Vaccination site rash
Symptomtext
rash kind of itches,; Delayed reaction; The injection site has a rash about the size of a couple of quarters; soreness in the arm for 2 days; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (soreness in the arm for 2 days), RASH PRURITIC (rash kind of itches,), SKIN REACTION (Delayed reaction) and VACCINATION SITE RASH (The injection site has a rash about the size of a couple of quarters) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. Concurrent medical conditions included Drug allergy (Lanolin), Allergy to antibiotic (Neomycin), Drug allergy (Pabrinex), Allergy to chemicals (MDGN), Drug allergy (balsam of peru), Allergy to chemicals (Propylene Glycol), Allergy to chemicals (Fragrance mixes), Allergy to chemicals (Compistane mix), Drug allergy (lidocaine), Allergy to chemicals (oak moss), Alcohol allergy (alcohol), Allergy to chemicals (Eugenol), Allergy to chemicals (Tea tree oil), Allergy to chemicals (sandalwood oil), Allergy to chemicals (lang lang oil) and Allergy to chemicals (hydroperoxide). On 11-Aug-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Aug-2021, the patient experienced PAIN IN EXTREMITY (soreness in the arm for 2 days). On 19-Aug-2021, the patient experienced RASH PRURITIC (rash kind of itches,), SKIN REACTION (Delayed reaction) and VACCINATION SITE RASH (The injection site has a rash about the size of a couple of quarters). On 13-Aug-2021, PAIN IN EXTREMITY (soreness in the arm for 2 days) had resolved. At the time of the report, RASH PRURITIC (rash kind of itches,), SKIN REACTION (Delayed reaction) and VACCINATION SITE RASH (The injection site has a rash about the size of a couple of quarters) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications include Primarin Cream Twice a week. No treatment information was mentioned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Alcohol allergy (alcohol); Allergy to antibiotic (Neomycin); Allergy to chemicals (Tea tree oil); Allergy to chemicals (sandalwood oil); Allergy to chemicals (Propylene Glycol); Allergy to chemicals (oak moss); Allergy to chemicals (MDGN); Allergy to chemicals (lang lang oil); Allergy to chemicals (hydroperoxide); Allergy to chemicals (Fragrance mixes); Allergy to chemicals (Eugenol); Allergy to chemicals (Compistane mix); Drug allergy (Pabrinex); Drug allergy (lidocaine); Drug allergy (Lanolin); Drug allergy (balsam of peru)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 17.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Heart rate
Heart rate increased
Myalgia
Pain in extremity
Pyrexia
Symptomtext
Soreness of arm; Fever; Body aches; Headache; Heart beat increased to 80-100 beats per minute; This spontaneous case was reported by a nurse and describes the occurrence of PAIN IN EXTREMITY (Soreness of arm), HEART RATE INCREASED (Heart beat increased to 80-100 beats per minute), PYREXIA (Fever), MYALGIA (Body aches) and HEADACHE (Headache) in a 19-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. Concomitant products included BIOTIN for an unknown indication. On 17-Aug-2021 at 11:30 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Aug-2021, the patient experienced HEART RATE INCREASED (Heart beat increased to 80-100 beats per minute). On 18-Aug-2021, the patient experienced PAIN IN EXTREMITY (Soreness of arm), PYREXIA (Fever), MYALGIA (Body aches) and HEADACHE (Headache). At the time of the report, PAIN IN EXTREMITY (Soreness of arm), HEART RATE INCREASED (Heart beat increased to 80-100 beats per minute), PYREXIA (Fever), MYALGIA (Body aches) and HEADACHE (Headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 17-Aug-2021, Heart rate: 80-100 (High) Fast heart beat around 6-7 PM 80-100 beats per minute. On an unknown date, Heart rate: 75-80 (normal) 75-80 beats per minute. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant drugs includes Birth Control No Treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Name: Heart beat; Result Unstructured Data: 75-80 beats per minute; Test Date: 20210817; Test Name: Heart beat; Result Unstructured Data: Fast heart beat around 6-7 PM 80-100 beats per minute
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- BIOTIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Myalgia
Pain
Vaccination site pain
Symptomtext
left arm was hurting, where I got the shot; body aches; headaches; muscle pain; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (body aches), HEADACHE (headaches), MYALGIA (muscle pain) and VACCINATION SITE PAIN (left arm was hurting, where I got the shot) in a 51-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 16-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Aug-2021, the patient experienced PAIN (body aches), HEADACHE (headaches) and MYALGIA (muscle pain). On 17-Aug-2021, the patient experienced VACCINATION SITE PAIN (left arm was hurting, where I got the shot). At the time of the report, PAIN (body aches), HEADACHE (headaches), MYALGIA (muscle pain) and VACCINATION SITE PAIN (left arm was hurting, where I got the shot) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication of the patient was not reported. On 16-Aug-2021, the symptoms started a little, but it started again on 17-Aug-2021 after work. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.09.2021
- Impfdatum
- 15.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Contusion
Symptomtext
A few hours after the injection, Pt started complaining of pain under her arm. Not at the injection site. The next evening, we noticed a large bruise under her arm. It spread from under her arm down to her breast.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- 200mg Lyrica 2x daily.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 03.09.2021
- Impfdatum
- 12.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Heart rate increased
Injection site pain
Pyrexia
Symptomtext
On 8/13/2021, 8/14/21 still feel heart elevated and fatigue. Fever, chills, elevated heart rate, fatigue, pain at injection sight. Felt like I had covid again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heart, Lipedema,allergies,
- Andere Medikamente
- None nothing.
- Allergien
- Lactose, ragweed, certain pollens, mold.
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 03.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Autism spectrum disorder
Injection site pain
Injection site swelling
Symptomtext
Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: Patient is autistic. Did not respond well to process of administering the vaccine (jumped away and tried to push me away with his other arm despite efforts to calm him). Vaccine was administered, but will likely be more sore due to how he responded to administration. Patient seemed fine and actually not even in pain at time of leaving 30 minutes after the vaccine was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 03.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Swelling face
Urticaria
Symptomtext
Hives and facial swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 02.09.2021
- Impfdatum
- 31.08.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Symptomtext
Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash Generalized-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 31.08.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Dizziness
Flushing
Hyperhidrosis
Tinnitus
Visual impairment
Symptomtext
Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Tinnitus-Medium, Systemic: Visual Changes/Disturbances-Mild, Systemic: Weakness-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 19.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypersensitivity
Infection
Peripheral swelling
Pruritus
Symptomtext
pt called on 9/1/2021 c/o allergic reaction and infection. hospitalized x 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- n/a
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 31.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Peripheral swelling
Symptomtext
Pt got her Vaccine on her right arm after a week she got her left arm swelling and pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- she is no
- Vorgeschichte
- High blood pressure, Osteoporosis, Sclerosis Spine , Osteoarthritis and glaucoma.
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.08.2021
- Impfdatum
- 29.08.2021
- Beginn
- 29.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Dysgeusia
Immediate post-injection reaction
Pain in extremity
Symptomtext
Metallic taste in mouth immediately after. Loss of smell and taste hours later. Arm soreness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamins. Claritin 10mg
- Allergien
- History of anaphylaxis to unknown allergen
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 30.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Musculoskeletal stiffness
Pain
Pyrexia
Symptomtext
8-12-2021 around 12 noon fever spiked to over 102, started alternating aleve and tylenol every four hours for six days, then arms aching from elbows to hands and legs from knees down to toes, joints on all constant stiffness. Spikes of headaches on and off the whole time. Last signs weened off 8-26-2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none didn't leave home
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- allergies
- Andere Medikamente
- B12 complex vitamin
- Allergien
- minocin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Rash
Symptomtext
Pt. states that after receiving the 1st dose of Moderna 08/13/2021. started experiencing symptoms 6hrs later, right hip (welps/hives), continuing to spread throughout the body. Some would disappear and new rashes would appear. Primary visit 08/18/2021 recommended steroid shot, Benadryl (continuing). Still continuing to appear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Valsartan, Lexapro, Tegretal, Attenial
- Allergien
- Lobster, Crab, Shrimp
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Rash
Symptomtext
Pt. states that after receiving the 1st dose of Moderna 08/13/2021. started experiencing symptoms 6hrs later, right hip (welps/hives), continuing to spread throughout the body. Some would disappear and new rashes would appear. Primary visit 08/18/2021 recommended steroid shot, Benadryl (continuing). Still continuing to appear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Valsartan, Lexapro, Tegretal, Attenial
- Allergien
- Lobster, Crab, Shrimp
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 29.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 12,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site rash
Injection site warmth
Rash erythematous
Rash macular
Symptomtext
Woke up with red blotchy rash on arm near injection site. Did not hurt or itch but occasionally it will itch a little. My shoulder would ache on and off. The rash got larger the next day. I put aloe gel, calamine lotion, triple antibiotic cream , hydrocortisone cream and iced it. Warm to the touch. Very concerned about this. No change.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None yet.
- Aktuelle Erkrankungen
- High blood pressure
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Metoprolol, iron pills, multivitamin, beets supplements, Claratin D as needed.
- Allergien
- Prednisone
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 27.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypoaesthesia
Muscular weakness
Pain in extremity
Symptomtext
Severe sharp pain with numbness and weakness on back/outside part of right thigh
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Inflammatory Polyarthritis
- Andere Medikamente
- Prednisone, Lexapro, Wellbutrin, Zyzal, Daily Vitamin
- Allergien
- Acetaminophen
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 15.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Myalgia
Pain
Symptomtext
body ache; started to feel real fatigued; muscle aches; had a headache; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (body ache), FATIGUE (started to feel real fatigued), MYALGIA (muscle aches) and HEADACHE (had a headache) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The patient's past medical history included COVID-19 in September 2020. Concomitant products included VITAMINS NOS and KRILL OIL for an unknown indication. On 15-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Aug-2021, the patient experienced PAIN (body ache), FATIGUE (started to feel real fatigued), MYALGIA (muscle aches) and HEADACHE (had a headache). On 17-Aug-2021, PAIN (body ache), FATIGUE (started to feel real fatigued), MYALGIA (muscle aches) and HEADACHE (had a headache) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- VITAMINS NOS; KRILL OIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 12.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Fatigue
Headache
Joint warmth
Malaise
Melanocytic naevus
Myalgia
Vaccination site swelling
Vaccination site warmth
Symptomtext
unwell; Swelling of mole on left elbow/Increased size of a mole on left elbow/now swelling, size has grown as a quarter/ mole described as size as a little pebble; Feels very weak; Hot to touch left elbow; Fatigue; Headache; Musclepain; Swelling at injection site; Hot to touch injection site; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (unwell), MELANOCYTIC NAEVUS (Swelling of mole on left elbow/Increased size of a mole on left elbow/now swelling, size has grown as a quarter/ mole described as size as a little pebble), ASTHENIA (Feels very weak), VACCINATION SITE WARMTH (Hot to touch injection site) and JOINT WARMTH (Hot to touch left elbow) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Penicillin allergy, Allergy to antibiotic (levoquine), Drug allergy (narcus), Allergy to antibiotic (microbid), Allergy to antibiotic (clindamycin), Drug allergy (lyrica), Drug allergy (haldol) and Drug allergy (ketamine). On 12-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Aug-2021, the patient experienced VACCINATION SITE WARMTH (Hot to touch injection site) and VACCINATION SITE SWELLING (Swelling at injection site). On 14-Aug-2021, the patient experienced MELANOCYTIC NAEVUS (Swelling of mole on left elbow/Increased size of a mole on left elbow/now swelling, size has grown as a quarter/ mole described as size as a little pebble), ASTHENIA (Feels very weak), JOINT WARMTH (Hot to touch left elbow), FATIGUE (Fatigue), HEADACHE (Headache) and MYALGIA (Musclepain). On an unknown date, the patient experienced MALAISE (unwell). On 13-Aug-2021, VACCINATION SITE WARMTH (Hot to touch injection site) and VACCINATION SITE SWELLING (Swelling at injection site) had resolved. At the time of the report, MALAISE (unwell), MELANOCYTIC NAEVUS (Swelling of mole on left elbow/Increased size of a mole on left elbow/now swelling, size has grown as a quarter/ mole described as size as a little pebble), ASTHENIA (Feels very weak), JOINT WARMTH (Hot to touch left elbow), FATIGUE (Fatigue), HEADACHE (Headache) and MYALGIA (Musclepain) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 15-Aug-2021: Significant follow-up received contains: added events-fatigue, headache, muscle pain, asthenia,malaise
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to antibiotic (microbid); Allergy to antibiotic (levoquine); Allergy to antibiotic (clindamycin); Drug allergy (narcus); Drug allergy (lyrica); Drug allergy (ketamine); Drug allergy (haldol); Penicillin allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site pain
Symptomtext
injection site soreness; exhaustion; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE PAIN (injection site soreness) and FATIGUE (exhaustion) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No medical history and laboratory data was provided by the reporter. On 09-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced INJECTION SITE PAIN (injection site soreness) and FATIGUE (exhaustion). At the time of the report, INJECTION SITE PAIN (injection site soreness) and FATIGUE (exhaustion) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. No treatment medications were reported. Patient stated to contact only through phone only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history and laboratory data was provided by the reporter.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Pain in extremity
Symptomtext
arm was sore; J&J vaccine on 09/Mar/2021, first dose of Moderna vaccine on 09/Aug/2021; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (arm was sore) and INTERCHANGE OF VACCINE PRODUCTS (J&J vaccine on 09/Mar/2021, first dose of Moderna vaccine on 09/Aug/2021) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 09-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Aug-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (J&J vaccine on 09/Mar/2021, first dose of Moderna vaccine on 09/Aug/2021). On 10-Aug-2021, the patient experienced PAIN IN EXTREMITY (arm was sore). On 09-Aug-2021, INTERCHANGE OF VACCINE PRODUCTS (J&J vaccine on 09/Mar/2021, first dose of Moderna vaccine on 09/Aug/2021) had resolved. At the time of the report, PAIN IN EXTREMITY (arm was sore) outcome was unknown. It was reported that patient received a dose of J&J vaccine on 09-MAR-2021, lot number: 1305029 for COVID-19 vaccination. No relevant concomitant medications were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 27.08.2021
- Impfdatum
- 24.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Chills
Headache
Nausea
Pain
Vomiting
Symptomtext
103.6 temp for 48 hours after shot. Severe body aches, chills, headache, nausea, vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Sinus infection
- Vorgeschichte
- Immunocomprmised. Single immune deficiency disorder.
- Andere Medikamente
- None
- Allergien
- Antibiotics
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 27.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Fatigue
Lethargy
Pain
Symptomtext
Systemic: Body Aches Generalized-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Joint Pain-Severe, Additional Details: Was given monoclonal antibody infusion 3 days post vaccination at healthcare center
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Skin lesion
Urticaria
Symptomtext
Red raised single hive/lesion 6? long by 3? wide, amorphous shape
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Treatment with Cefdinir and Doxycycline
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lupus, Depression
- Andere Medikamente
- Plaquenil, Lisinopril, Lexapro, Trazodone, Meloxicam, L-Lysine, Black Seed Oil, Biotin, Centrum, Calcium/Magnesium
- Allergien
- Codeine
- Vorherige Impfungen
- Joint pain after 2nd COVID vaccine
- Staat
- NE
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 23.08.2021
- Beginn
- 24.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Rash
Rash pruritic
Symptomtext
After about 24 hours after recieving the second shot, I noticed a rash forming on my arm. It?s now been 48 hours after the shot and the rash is growing larger. It itches and burns slightly, but not to the point where it is unbearable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal Vitamin
- Allergien
- Gluten & Dairy
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Swelling
Symptomtext
The next day I was experiencing severe itching all over my body and then the day after that I experienced rashes on my arms and swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Nexplanon birth control implant
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 19.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Myalgia
Pain in extremity
Pyrexia
Symptomtext
Patient report that she has muscle pain on her left side all the way down to her feet... also reported that she had a fever and numbness in her leg.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 12.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Liver function test
Rash
Symptomtext
Patient reported getting a rash around the neck area the day after receiving the vaccine. She self treated with a cold compress and cool water. She contacted her prescriber when the rash began to spread to her face, ears and arms. The prescriber gave a script for Prednisone. Prescriber is also doing blood work to check liver function due to Dress Syndrome.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DRESS syndrome
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Fatigue
Headache
Nausea
Pain
Pyrexia
Symptomtext
Heart beating hard, normal heart rate, just felt it was beating hard.(4 hrs after receiving shot). 16 hours after receiving 2nd vaccine shot: Fatigue Severe headache Fever Body aches Sore arm (left arm received vaccine in). Nausea Loss of appetite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic back pain
- Andere Medikamente
- -
- Allergien
- Augmentin, zophran, toroidal
- Vorherige Impfungen
- Headache, fatigue, fever, sore arm
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 22.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Injection site pain
Lethargy
Musculoskeletal stiffness
Symptomtext
Chills, lethargy, sore arm at int. site muscle stiffness. Felt better this a.m. 8/24/2021. Improving
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- COPD, Diabetes, peripheral neuropathy, Carotid stenosis right
- Vorgeschichte
- COPD, Diabetes, peripheral neuropathy
- Andere Medikamente
- Supplemental Oxygen 3 liters at night Fasenra every 2 months injection started Feb 23 2021 Nebulizers Budesonide 0.5 mg Perforomist 20MCg Yupelri 175MCg/3Ml Azithromycin 250mg Mon, Wed & Fri Singulair p.m Gabapentin 300 mg a.m
- Allergien
- Levaquin Vancomyacin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 18.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Fatigue
Fear
Feeling abnormal
Headache
Heart rate increased
Injection site pain
Myalgia
Symptomtext
I had the normal predicted pain at the injection site, tiredness, headache, muscle pain, chills, and joint pain. But I also experienced a very rapid heart rate with minor activity that morning, that made me feel like I was going to give out. It scared me pretty bad. My heart rate jumped to 154 and stayed that way until I would sit for an extended period. I did notice on my watch that it stayed higher than normal that whole day. I stayed pretty tired for about 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- no
- Andere Medikamente
- Tri-Lo Birth control, zyrtec, multivitamin, vitamin c
- Allergien
- lactose, pineapple, figs
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pyrexia
Symptomtext
Fever and tired lasted 4-5 hours. I drank fluids and rested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- EDS, MS, A-Fib, Hypertension, Breast Cancer, Hashimotos
- Andere Medikamente
- Gabapentin, Metoprolol, Atorvastatin, Levothyroxine, Amlodipine, Multi-Vitamins, B12, D
- Allergien
- Sulfur, Aspirin, NSAIDS, Penicillin, Nyacins
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 19.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site swelling
Injection site warmth
Symptomtext
Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: patient called store on Saturday August 21 to tell me she had a reaction to the shot. She said it was hot, red and swollen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 22.08.2021
- Impfdatum
- 21.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Moderna Covid-19 Vaccine EUA :Injection site reaction. Started with mild itching the same afternoon. I woke up at 1 am this morning to find the area around the injection site, 6 inches in diameter, red, hot and swollen, area firm to touch. Benadryl had no effect. Will be taking 5 mg prednisone p.o., and also icing down next.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood pressure, and high cholesterol
- Andere Medikamente
- Temisartan 80 mg qd, Rosuvastatin 20 mg qd, Qunol 100 mg qd, Calcium with wiht Vit D, Magnesium, Zinc, Omega -3, 2100 mg, Vitamin C 500 mg. Loratadine 10 mg, Benadryl 25 mg PRN
- Allergien
- sulfa compounds, such as Bactrim
- Vorherige Impfungen
- Chills and body aches, age 68, Moderna #2, 3/15/2021
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 21.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site hypersensitivity
Injection site warmth
Symptomtext
allergic reaction at injection site, red and warm to the touch,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 21.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
Itching all over body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Hyperhidrosis
Oral pruritus
Symptomtext
patient received vaccine at 10:55am, waited 15 minutes, stated she felt fine, left the facility. at 12:22pm a representative called on behalf of the patient because the patient speaks broken english. the representative stated the patient was experiencing an itchy mouth and ears and sweating profusely. I asked if the patient was having shortness of breath. The representative replied that they were texting back and forth and when she asked her that question the patient responded "in my chest". I advised that the patient call 911 or seek immediated medical attention
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 19.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Pyrexia
Symptomtext
Low Grade fever, joint soreness, soreness at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None to date
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Covid diagnosed on June 14
- Andere Medikamente
- Vitamins A, C, D, E, Biotin, Melatonin, Iron, Omega-3 Fish Oil, Atvorstatin, Losartin, Fluticosone, Adapaleine (nasal sprays)
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 19.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
I had my shot over a week ago and today the injection site has gotten red, swollen and itchy. It continues to get larger. I am planning to call the doctor tomorrow if it's not better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Meniere's Disease Brain Aneurysm
- Andere Medikamente
- Multi vitamin
- Allergien
- Nystatin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 18.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site pain
Injection site pruritus
Injection site rash
Injection site warmth
Rash erythematous
Symptomtext
Rash on left arm where shot was given but expanding beyond it. Rash red with a slightly dark red outlining the outside of the rash. Hot to the touch, slight itching but more of a burning sensation. Itching/burning sensation being mild.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic sinusitis, general anxiety disorder
- Andere Medikamente
- Ibuprofen / daily multivitamin
- Allergien
- Lactose intolerant, latex allergy, seasonal allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 18.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Developed hives on left side of neck approximately 3 to 4 hours after receiving shot , took Benadryl, hives disappeared after 1 hour of taking medicine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 14.08.2021
- Impfdatum
- 12.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Balance disorder
Constipation
Dizziness
Headache
Symptomtext
HEADACHE, DIZZINESS, OFF BALANCE, CONSTIPATED, INCREASED BLOOD PRESSURE, EMERGENCY ROOM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site rash
Injection site swelling
Symptomtext
After 7 days, on August 12th, I starting feeling pains around the shot area and it was severely itchy. When I finally took a look at it, it was a red, swollen and rash-like spot, measuring about 2 inches and round in shape.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Tricuspid Heart valve regurgitation Hashimoto disease, hyperthyroidism
- Andere Medikamente
- -
- Allergien
- Amoxicillin, clindamycin, vancomycin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site warmth
Symptomtext
There is a red circle approx two inches wide surrounding the injection site. The red area is warm to the touch and itchy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Fibromyalgia
- Andere Medikamente
- Celexa
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 07.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Rash
Symptomtext
Patient reports "covid arm", Rash, redness and itching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Unspecified Cancer
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 12.08.2021
- Impfdatum
- 12.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 12.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Urticaria
Vomiting
Symptomtext
She had a whelp on her arm about 2 inches in diameter. she said she had been throwing up since she got the shot. She stated her arm hurt very much.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- unknown
- Andere Medikamente
- Phentermine, Depo-Provera, Aimovig, Keppra,
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 12.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Diarrhoea
Ear pain
Headache
Injection site pain
Lymphadenopathy
Pain
Pain in extremity
Pyrexia
Skin warm
Tenderness
Symptomtext
arm tenderness, pain and warmth. swollen lymph nodes on left side of the neck along with tenderness in that area. pain in shoulder and scapula area on left side{side where injection was}. all over body aches, headache, ear ache, chills, fever and diarrhea. the very first symptoms were injection site pain and the swollen lymph nodes with in an hour of injection. headache and ear ache come on about 6hrs after followed shortly by diarrhea. the following day began chill and all over body ache along with previous symptoms. diarrhea had subsided by then. fever did not spike until nearly 24hrs later but only lasted a few hours. by the 48hr mark. symptoms have lessened but not completely gone. arm, neck shoulder pain remains the same as well as the swollen lymph nodes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- after the first does i had the swollen lymph nodes. i had and ultra sound and chest ct with contrast. they did find 3 swollen lymph nodes but the did not appear concerning.
- Aktuelle Erkrankungen
- a cold, covid test was negative about 4wks prior
- Vorgeschichte
- asthma alpha1 antitrypsin deficiency obesity
- Andere Medikamente
- phentermine 37.5 mg 1/2 pill daily, topiramate 25mg 1 pill daily, zafirlukast 20mg 2x daily, spiriva 2.5 2puffs once a day, vitamin d3 2000 iu once a day
- Allergien
- percocet, montelukast, codeine, inhalation corticosteroids, steri strips
- Vorherige Impfungen
- moderna covid vaccine 1st does
- Staat
- KS
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 12.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Pain in extremity
Vaccination site rash
Vaccination site swelling
Vaccination site warmth
Symptomtext
Rash where the vaccine was administered, pain, swollen and warm to touch. Client also complained that she started having pain in right arm that was consistent and is still bothering her. Allergy medicine and tylenol/ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Tylenol, Ibuprofen, Claritin
- Allergien
- Penicillin, Adhesive Latex, Lavender
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 11.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Glossodynia
Pain in extremity
Symptomtext
about 10 MiNutes after pt. received the shot, they started coMplaiNiNg about paiN iN their right arM, right leg and toNgue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NoNe
- Vorgeschichte
- aNgiNa
- Andere Medikamente
- MirtazapiNe 30 Mg, Keppra 500 mg, famotidine
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 11.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
BUMPS AND HIVES on the opposite arm of the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Malaise
Symptomtext
feeling uneasy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Daily Atorvastatin, Amlodipine, Zinc, vitamin B1, and Magnesium
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 11.08.2021
- Impfdatum
- 30.07.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash vesicular
Symptomtext
per pt 1 week post vaccine she noticed a "chickpox" like rash on her legs, that also somewhat spread to her bra line. she said she has taken some zyrtec and it has helped slow the spread but that it is has not gone away and seems blister like.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- per pt none
- Vorgeschichte
- smoker
- Andere Medikamente
- unknown
- Allergien
- aspirin, codeine, air bourne
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- FINASTERIDE, LANSOPRAZOLE, ADDERALL, COLESTIPOL, HYDROXYZINE
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 11.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fatigue
Headache
Nausea
Pyrexia
Symptomtext
Fever, fatigue, headache, nasuea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 11.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Injection site red, swollen, itchy, tender
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, eczema
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 10.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Furuncle
Rash
Symptomtext
WITHIN 24 HOURS OF RECEIVING THE VACCINATION SHE GOT BOILS OR BUMPS UNDER HER ARMPIT. HAD TO SEE A MD AND THE MD PRESCRIBED HER ANTIBIOTICS. STILL TAKING ANTIBIOTICS AND HAS A FOLLOW UP WITH HER MD AS THE BOILS/BUMPS ARE STILL THERE/HEALING.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 10.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cellulitis
Erythema
Injection site erythema
Injection site pain
Pain in extremity
Peripheral swelling
Symptomtext
Pt received second Moderna vaccine on 8/3 and on 8/4 developed redness and pain at the injection site. She presented to our ER on 8/8 c/o arm being red, swollen and painful. She was given 1gm ancef IM and d/c with tylenol #3 and bactrim rx. She returned to the ER on 8/9/21 with increased swelling, pain and redness concerning for cellulitis. She was given fluids, zosyn and admitted to med surg for observation with diagnosis of cellulitis in the left upper arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN
- Andere Medikamente
- Lisinopril 10mg tab daily,
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 09.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Nausea
Retching
Symptomtext
upon screening patient he informed that he had a fear of needles. After the immunization was given patient felt like he was going to throw up. Immediately got patient a waste back in case he was going to throw up. Patient dry heaved once but never vomited. Pt felt hot. We attempted to give patient an ice pack but he requested a fan , we got a fan and that helped. Pt's dad was present so we asked dad to come in the room to comfort and sooth patient. Pt requested water so we gave him a bottle of water. We had patient sit for 25-30 minutes. pt left without incident. called pt this evening and he said he was feeling better, was a little nauseous the rest of the day but was able to eat lunch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 09.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Injection site bruising
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Pyrexia
Symptomtext
PATIENT GOT VACCINE ON 8/5/21 AND CAME ON 8/9/2021 TO PICK UP ANTI BIOTIC AND HAD CONVERSATION THEN FIND OUT ABOUT HER REACTION. SHE HAD SMALL BRUISE ON HER LEFT ARM AT INJECTION SITE, HER AREA OF VACCINATION IS SWALLON, RED AND HOT. SHE STARTED FEVER NEXT DAY, SHE STATED THAT SHE DID TOOK TYLENOL 500MG EVERY 6 HOURS TO HELP, BUT IT WAS ON AND OFF. SHE FELT LIKE ALLERGIC REACTION ALL OVER HER BODY AND HAVING ITCH AT INJECTION SITE AND OTHER AREAS OF BODY. SHE WENT TO PRIMARY CARE DOCTOR TODAY, AND SHE WAS TOLD TO FINISH BACTRIM DS FOR 10 DAYS, BENDRYL AND TYLENOL UNTIL SYMTOMPS GETS BETTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- SHE HAD BRAIN TUMOR BUT NOT ANYMORE PER IN PERSON TALK, AND SHE REPORTED OF LIVER ISSUE (DOES NOT KNOW WHAT IT IS)
- Vorgeschichte
- CHRONIC PAIN DUE TO TUMOR
- Andere Medikamente
- NONE
- Allergien
- NOT LISTED ON IMZ FORM
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 09.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mass
Pain in extremity
Symptomtext
Patient returned to pharmacy about 30 minutes after vaccination with complaint of minor pain in left forearm and being able to feel a mass in forearm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 08.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Nausea
Pain
Pyrexia
Symptomtext
Fever up to 102.7 (with taking Tylenol every 4 hours) nausea, headaches, extremely bad body aches to where I could barely get out of bed, fatigue. Fever stayed that high for about 20 hours, then 100 temp the next day and symptoms less severe, the 3rd day fever was 99 and less symptoms. I sought no further care from health provider and by 4th day back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 08.08.2021
- Impfdatum
- 07.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pyrexia
Vomiting
Symptomtext
after dinner , fever, took Tylenol. went home overnight vomited and went back to sleep. woke up in the morning still feeling fatigued. did not eat , did not take temperature again and did not take any more tylenol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Covid positive 07/2021
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 06.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
Redness and mild swelling on injection site. About a 3-4 inch diameter redness area. Patient still able to ambulate and talk. No sign of allergic reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Phenergan
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 06.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Muscular weakness
Nausea
Pain in extremity
Symptomtext
soreness in right arm, numbness in right hand, having a hard time with opening and closing right hand and nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 05.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lip swelling
Urticaria
Symptomtext
pt's lips swelled and she developed hives
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none that she reported
- Vorgeschichte
- none that she reported
- Andere Medikamente
- Singular 10 mg 1qd.
- Allergien
- eggs
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 05.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Hives started about 5 minutes after immunization. Gave 50 mg of Benadryl and ice to apply to skin. No progression of symptoms. Stayed in store about 45 minutes total. Said she felt fine and left with person she came with. Said she wanted to take cool shower and he promised to watch for any other symptoms. Phone calls confirmed she is fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension
- Andere Medikamente
- amlodipine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 05.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Impaired driving ability
Nausea
Symptomtext
About 5 minutes after administration of the vaccination, patient became nauseated and was coughing a little, and had to lie down. The patient's breathing was fine but he felt mostly nauseated which lasted for at least 30 minutes after he first told the staff he was nauseated. We monitored patient while lying down, got a fan to put on him and after about 5 minutes of lying down, the patient sat back up in chair at immunization table and put a fan at table for him, he asked for water and some crackers which we gave him and he did eat and drink. He texted his wife to come pick him up as we felt it may be unsafe for him to drive his 20 minute commute back home, his wife came approximately 40 - 45 minutes after his initial symptoms and by that time he was much better and walked out of the pharmacy area without assistance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- not available
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 05.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Exposure during pregnancy
Fatigue
Symptomtext
One or two hours after the vaccination the patient said she started to fell quite tired. I called her back a couple of times to see how she was doing and she says she is a lot better. She is also pregnant, so I do not know if this is related to pregnancy or vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 03.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Hyperhidrosis
Vomiting
Symptomtext
Patient received Moderna COVID-19 vaccine today 8/3/2021 around 3:45 pm. Patient mentioned in the past she gets dizzy and lightheaded after any vaccine. The pharmacist asked her to stay seated in the chair after the vaccine (rather than getting up and walking outside the room to sit in one of the chairs outside). After the vaccine, patient felt a little dizzy and was sweating. Pharmacist offered an ice pack, which she used and it helped. She said she felt fine, so pharmacist told her she would check on her in a few minutes. Around 3:50 pm, mom was with the patient and told pharmacist patient was throwing-up. She was given a bag and paper towels. She felt good after she threw-up. Pharmacist checked her blood pressure around 3:52 pm. It was 83/50 and pulse 59. She did not know her normal blood pressure. Patient stayed until around 4:10 pm. She felt a lot better. The mom and sister were with patient to accompany her. Pharmacist called patient around 7:45 pm and confirmed with patient that she was feeling okay. Patient stated she was feeling fine. No more dizziness or throwing-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Dizziness.
- Staat
- AL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 03.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Nausea
Symptomtext
patient said she felt faint and nauseous- no treatment done. offered to call ambulance, patient refused
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Unresponsive to stimuli
Symptomtext
patient and her husband came into pharmacy for their 1st dose of moderna covid19 vaccine. they expressed that they're very anxious and nervous about getting the vaccine and waited this far to get it. I gave the patient the shot at 12:40pm and right after the shot she excitedly stated "wow, I did not feel anything at all. thank you!". I then told her to join her husband and have a seat at the post-vaccination monitoring area. At 12:51, I checked her on her and husband. Her husband stated that she was happy when she got out of the room but now it looks like she's very tired and not responding to him when he asked her some questions. I made a suggestion to give her some water and to have him taking back to our immunization room so it's more private for her to rest. He had to dragged her into the room while I carried her back. He then said please call paramedics because it seems like she's passing out. Our pharmacy staff checked with her husband again to make sure he wanted us to dial 911. At soon as he said yes ! please call 911, she suddenly gained consciousness, opened her eyes and started talking and told us she wants a soda. We tried to check her blood pressure with the automated machine and it read 75/57 twice. We gave her some chips and soda to help. She spent over 1 hour in our room then stated she felt much better and left with her husband around 2 pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- N/A
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 31.07.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Hyperhidrosis
Hypotonia
Symptomtext
AFTER THE PATIENT HAD BEEN SITTING IN THE WAITING AREA ABOUT 8-10 MINUTES I LOOKED UP FROM DRAWING MORE VACCINES TO DISCOVER THE PATIENT'S HUSBAND HOLDING THE PATIENT WHO WAS SLUMPED IN HER CHAIR. WHEN HE SAW ME LOOKING HE WAVED HIS HAND AND SAID SHE'S OK , SHE'S FINE. I DROPPED WHAT I WAS DOING AND WENT OUT TO CHECK ON HER. HE STATED SHE DOES THIS ANYTIME SHE GETS A SHOT AND SAID SHE'D BE OK IN A MINUTE. I ASKED IF HE WANTED ME TO CALL AN AMBULANCE TO CHECK HER OUT. HE SAID NO, YOU JUST HAVE TO GIVE HER A MINUTE. HE STATED HE'D BEEN THROUGH THIS WITH HER MANY TIMES BEFORE. I GOT HIM A DAMP PAPER TOWEL AND AND CARD TO FAN HER WITH, SINCE SHE WAS SWEATY. THE PATIENT PERKED UP IN A FEW MINUTES. SHE SAID SHE FELT OK AND I THEN HAD MY TECHNICIAN TAKE HER SOME WATER. I FOLLOWED UP WITH THE PATIENT THE FOLLOWING DAY AND SHE STATED SHE WAS DOING FINE BUT THAT THE VACCINE HAD KIND OF "ZAPPED" HER. SHE STATED SHE HAD A COUPLE OF THE EXPECTED SIDE EFFECTS HEADACHE AND FATIGUE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none per patient
- Vorgeschichte
- none per patient
- Andere Medikamente
- none per patient
- Allergien
- none per patient
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 01.08.2021
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Nausea
Vomiting
Symptomtext
Patient reported previous sensitivity/syncope to vaccines. Waited the required 15 minute time post vaccination and had a seat with her legs elevated, felt anxious, and fell suddenly nauseous and vomited in the immunization administration area. Pharmacist helped clean up, offered emergency services to patient which were declined. Took some time to clean up and we provided comfort measures while she recovered. Following vomiting episode patient was ok to leave the area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 01.11.2023
- Impfdatum
- 15.11.2021
- Beginn
- 15.05.2022
- Tage bis Beginn
- 181,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
COVID-19; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (COVID-19) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 048221A and 939902) for COVID-19 prophylaxis. The patient's past medical history included Hysterectomy (partial) in 2014. Previously administered products included for Product used for unknown indication: Pfizer (EN6204) on 26-Mar-2021 and Pfizer (EWaSO) on 17-Apr-2021. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. Concurrent medical conditions included High cholesterol (05-Unk-2005, Under control w/current medications) and Endometriosis (In 2014 partial hysterectomy & Noretindrone until 6/23 kept it at bay until approx. 2 weeks after 9/27/23 booster) since 1997. On 15-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Apr-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 15-May-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced COVID-19 (COVID-19). At the time of the report, COVID-19 (COVID-19) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 15-May-2022, SARS-CoV-2 test: Positive. No concomitant medications were reported. No treatment medications were reported. This case was linked to MOD-2023-746576 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220515; Test Name: COVID-19; Test Result: Positive
- Aktuelle Erkrankungen
- Endometriosis (In 2014 partial hysterectomy & Noretindrone until 6/23 kept it at bay until approx. 2 weeks after 9/27/23 booster); High cholesterol (05-Unk-2005, Under control w/current medications)
- Vorgeschichte
- Medical History/Concurrent Conditions: Hysterectomy (partial)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 01.06.2023
- Impfdatum
- 01.06.2023
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Blood test
Magnetic resonance imaging
Multiple sclerosis
Neck surgery
Symptomtext
I FELL IN DEC 2021 AND BROKE MY WRIST AND HAD TO HAVE SURGERY AND NOW I HAVE NO BALANCE AT ALL. MY PC IS SURE I HAVE MS AND GETTING READY TO SEE A NEUROLOGIST
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- 2,0
- Labordaten
- MRI'S, BLOODWORK, SURGERY ON NECK
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- BP
- Andere Medikamente
- losartan, protonix, flonase, zyrtec, synthroid,
- Allergien
- morphine, demeral, reglan, codeine,
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 25.04.2023
- Impfdatum
- 08.11.2021
- Beginn
- 23.04.2022
- Tage bis Beginn
- 166,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Coagulopathy
Hypoxia
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE COAGULOPATHY, UNSPECIFIED TYPE HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coagulopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 12.03.2023
- Impfdatum
- 08.09.2021
- Beginn
- 09.03.2023
- Tage bis Beginn
- 547,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
patient hospitalized.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 08.02.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Product dose omission issue
Symptomtext
covid 19; patient never went back to receive the second dose in her Primary Series; This spontaneous case was reported by an other health care professional and describes the occurrence of COVID-19 (covid 19) and PRODUCT DOSE OMISSION ISSUE (patient never went back to receive the second dose in her Primary Series) in an adult female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. In 2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COVID-19 (covid 19) and PRODUCT DOSE OMISSION ISSUE (patient never went back to receive the second dose in her Primary Series). At the time of the report, COVID-19 (covid 19) and PRODUCT DOSE OMISSION ISSUE (patient never went back to receive the second dose in her Primary Series) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. The patient never went back to receive the second dose in Primary Series of the Moderna Covid-19 vaccine. It would be more than 35 days between Moderna Covid-19 Primary Series doses. Treatment medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 08.09.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 174,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
lot 042J21A should have been reported with a BUD of Feb 17, 2022.; No adverse event; lot 042J21A should have been reported with a BUD of Feb 17, 2022.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (lot 042J21A should have been reported with a BUD of Feb 17, 2022.), PRODUCT STORAGE ERROR (lot 042J21A should have been reported with a BUD of Feb 17, 2022.) and NO ADVERSE EVENT (No adverse event) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 042J21A and 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Mar-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 01-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (lot 042J21A should have been reported with a BUD of Feb 17, 2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (lot 042J21A should have been reported with a BUD of Feb 17, 2022.) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (lot 042J21A should have been reported with a BUD of Feb 17, 2022.), PRODUCT STORAGE ERROR (lot 042J21A should have been reported with a BUD of Feb 17, 2022.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (lot 042J21A should have been reported with a BUD of Feb 17, 2022.) and PRODUCT STORAGE ERROR (lot 042J21A should have been reported with a BUD of Feb 17, 2022.). Concomitant products were not provided. Treatment medication were not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow-up contains no new information.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 22.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in an 86-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). Concomitant product use was not provided by the reporter. lot 939902 reported with a BUD of 02-Sep-2021. Treatment information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live follow-up received included non significant information.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 15.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date) and NO ADVERSE EVENT (No adverse event) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date). No concomitant medication was reported. Pharmacist reported that they have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 days beyond use date. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live Significant Follow-up received; Patient information and vaccinations details updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 15.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date) and NO ADVERSE EVENT (No adverse event) in a 23-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patients had been administered with the Moderna vaccine (more or less 170 monovalent) which were beyond the 30 days beyond use date). No concomitant medication was reported. Pharmacist reported that they have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 days beyond use date. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live Significant Follow-up received; Patient information and vaccinations details updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 08.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 60-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Sep-2021, the patient received second dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 08-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). No concomitant information was reported. BUD reported as 02Sep2021. No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Non-significant Live follow-up.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 06.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 33-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 06-Oct-2021, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 06-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date). No concomitant information was reported. BUD reported as 02Sep2021. No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live follow-up Appended.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 08.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.), PRODUCT STORAGE ERROR (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.), PRODUCT STORAGE ERROR (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and PRODUCT STORAGE ERROR (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). No concomitant medication information was provided. The vaccine BUD was reported as 02Sep2021. Treatment medication information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Non significant live follow up received.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 06.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date; No adverse event; Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date), PRODUCT STORAGE ERROR (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 06-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date), PRODUCT STORAGE ERROR (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and PRODUCT STORAGE ERROR (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date). No concomitant medication information was provided. The vaccine BUD was reported as 2Sep2021. Treatment medication information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Non significant Follow up received.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 06.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patient administered with the Moderna vaccine, which were beyond the 30 day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine, which were beyond the 30 day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 44-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 06-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine, which were beyond the 30 day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine, which were beyond the 30 day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine, which were beyond the 30 day beyond use date.). Concomitant product use was not provided by the reporter. Patients administered Moderna vaccine monovalent beyond the 30 day beyond use date. Batch number 939902 (BUD - 02Sep2021). No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Non significant Follow up Appended; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patient administered with the Moderna vaccine, which were beyond the 30day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine, which were beyond the 30day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine, which were beyond the 30day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine, which were beyond the 30day beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine, which were beyond the 30day beyond use date). Concomitant product use was not provided by the reporter. Patients administered Moderna vaccine monovalent beyond the 30 day beyond use date. Batch number 939902 (BUD - 02Sep2021). No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live significant follow up: Updated narrative.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use) and NO ADVERSE EVENT (No adverse event) in an 83-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use). No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use) and NO ADVERSE EVENT (No adverse event) in an 89-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use). No concomitant medications were reported. Pharmacist reported that they have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 days beyond use date. The lot number for the monovalent vaccines with their corresponding BUD dates were 027C21A (BUD - 21-May-2021), 053C21A (BUD - 01-Jul-2021), 939902 (BUD - 02-Sep-2021), 011F21A (BUD - 04-Nov-2021), 012H21B (BUD - 23-Dec-2021), 056M21A (BUD - 12-May-2022), 082B22A (BUD - 08-Sep-2022). The lot numbers for the bivalent vaccines with their corresponding BUD dates and the interval period of administration. 052D22A (BUD - 17-Nov-2022), dates of administration 18-Nov-2022 to 28-Nov-2022, 023H22A, (BUD - 15-Dec-2022), dates of administration 16-Dec-2022 to 20-Dec-2022. It was reported lot 042J21A should have been reported with a BUD of 17-Feb-2022. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live significant follow up contains updated narrative.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 20-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). No concomitant medicine were reported. No treatment medicine were reported. lot 042J21A should have been reported with a BUD of 17-Feb-2022. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live significant follow up: Updated narrative.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 58-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). No concomitant medicine were reported. No treatment medicine were reported. lot 042J21A should have been reported with a BUD of 17-Feb-2022. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live significant follow up: Updated narrative.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- U
- Eingang
- 31.01.2023
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 58-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). No concomitant medicine were reported. No treatment medicine were reported. lot 042J21A should have been reported with a BUD of 17-Feb-2022. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live significant follow up: Updated narrative.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 41-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 24-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). No concomitant medicine were reported. lot 042J21A should have been reported with a BUD of 17-Feb-2022. No treatment medicine were reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live significant follow up: Updated narrative.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 29.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 day beyond use date). No concomitant medication were reported. Pharmacist reports that they have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 monovalent and 20 bivalent) which were beyond the 30 day beyond use date. The BUD for lot number 939902 was reported as 02-Sep-2021. No treatment information was provided by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Live follow up received with Updated narrative.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 22.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Patient administered with the Moderna vaccine which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Patient administered with the Moderna vaccine which were beyond the 30day beyond use date.). Concomitant drugs were not reported. It was reported that more or less 192 patients had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30 day beyond use date. Beyond use date for the monovalent vaccine with Lot number 939902 was reported as 02-Sep-2021. Treatment medications were not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow-up received contains non-significant information.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 22.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) in a 79-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 042J21A and 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Mar-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 22-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (They have more or less 192 patients who had been administered with the Moderna vaccine (more or less 170 -monovalent and 20 bivalent) which were beyond the 30day beyond use date.). No concomitant medications were reported. It was reported that lot 042J21A should have been reported with a BUD of Feb 17, 2022. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416, US-MODERNATX, INC.-MOD-2023-704486 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Livefollow up: Updated narrative.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case US-MODERNATX, INC.-MOD-2023-704486:dose 4 (bivalent drug)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 22.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Vaccine BUD was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021; No adverse event; Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date), PRODUCT STORAGE ERROR (Vaccine BUD was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021) and NO ADVERSE EVENT (No adverse event) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine BUD was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date), PRODUCT STORAGE ERROR (Vaccine BUD was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and PRODUCT STORAGE ERROR (Vaccine BUD was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021). Concomitant medications details were not reported by the reporter. Treatment details was not reported by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow-up received contains narrative updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 15.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Vaccine was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021; No adverse event; Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date), PRODUCT STORAGE ERROR (Vaccine was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021) and NO ADVERSE EVENT (No adverse event) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Sep-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date), PRODUCT STORAGE ERROR (Vaccine was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and PRODUCT STORAGE ERROR (Vaccine was reported 02-Sep-2021 which was administered to patient on 22-SEP-2021). No concomitant medication was reported. No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow up received included narrative information updated.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416: case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 15.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Moderna vaccine (more or less 170 - monovalent and 20 bivalent) which were beyond the 30 day beyond use date). No concomitant drug was reported. The before use date was 02-Sep-2021. No treatment drug was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-704416 (Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Jan-2023: Follow-up received contains non-significant information.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-704416:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 02.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
contracted Covid-19; This spontaneous case was reported by an other health care professional and describes the occurrence of COVID-19 (contracted Covid-19) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 004F21A. and 939902) for COVID-19 prophylaxis. No Medical History information was reported. On 02-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Oct-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced COVID-19 (contracted Covid-19). At the time of the report, COVID-19 (contracted Covid-19) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. The patient received her first dose of Moderna Covid-19 vaccine on 2OCT2021 lot number 939902 expiration date was not known. No expiration date was provided. The caller reports that her daughter contracted Covid-19 at some point after the first dose. The patient received her second dose of the Moderna Covid-19 vaccine on 30OCT2021 lot number 004F21A. No expiration date was provided. Caller was not sure if her daughter had any adverse reactions. The caller said that she did not know if her daughter received any Moderna booster doses. No treatment was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 27.11.2021
- Beginn
- 02.01.2023
- Tage bis Beginn
- 401,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case dose 1 Moderna 3/9/21 040A21A dose 2 Moderna 4/6/21 045A21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 1/2/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 29.12.2022
- Impfdatum
- 21.09.2021
- Beginn
- 10.08.2022
- Tage bis Beginn
- 323,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
Patient was diagnosed and hospitalized while vaccinated for COVID 19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 28.09.2022
- Impfdatum
- 28.10.2021
- Beginn
- 15.09.2022
- Tage bis Beginn
- 322,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 9/14/2022 - 9/17/2022 Presentation to the ED: COVID-19 + date: 9/15/22. Treatment: SUPPLEMENTAL O2. NO REMDESIVIR OR DECADRON. Discharge to: Home or Self Care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, CHRONIC RESPIRATORY FAILURE, RECURRENT UTIS, GERD, DEPRESSION, ANXIETY.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 24.09.2022
- Impfdatum
- 05.08.2021
- Beginn
- 08.02.2022
- Tage bis Beginn
- 187,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Gastric disorder
Inappropriate schedule of product administration
Nephrolithiasis
SARS-CoV-2 test
Symptomtext
Kidney stones; gastric issues; Took first dose on 05-Aug-2021 and second dose on 13-Sep-2021; Tested positive for COVID-19; This spontaneous case was reported by an other health care professional and describes the occurrence of NEPHROLITHIASIS (Kidney stones) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 020F214, 020F128 and 939902) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect products included non-company products ENCORAFENIB (BRAFTOVI) capsule for Cancer and CETUXIMAB (ERBITUX) for Cancer. Concurrent medical conditions included Colorectal cancer stage III since November 2017. In 2021, the patient ENCORAFENIB (BRAFTOVI) (Oral) dosage was changed to 75 milligram four times per day. On 05-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 29-Sep-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient started ENCORAFENIB (BRAFTOVI) (Oral) at an unspecified dose and CETUXIMAB (ERBITUX) (Intravenous) at an unspecified dose every two weeks. On 08-Feb-2022, the patient experienced COVID-19 (Tested positive for COVID-19). On an unknown date, the patient experienced NEPHROLITHIASIS (Kidney stones) (seriousness criterion medically significant), GASTRIC DISORDER (gastric issues) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Took first dose on 05-Aug-2021 and second dose on 13-Sep-2021). At the time of the report, NEPHROLITHIASIS (Kidney stones) and GASTRIC DISORDER (gastric issues) outcome was unknown, COVID-19 (Tested positive for COVID-19) had not resolved and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Took first dose on 05-Aug-2021 and second dose on 13-Sep-2021) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 08-Feb-2022, SARS-CoV-2 test: (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Company comment: This is a spontaneous case concerning a 77-year-old female patient with Colorectal cancer stage III on treatment with encorafenib and Erbitux, who experienced the non-serious unexpected AESI COVID-19, on an unknown lapse of time after receiving the booster dose of mRNA-1273. Patient was tested positive twice and reported had no symptoms. Inappropriate schedule of product administration was also captured as an event. The benefit-risk relationship of mRNA-1273 is not affected by this report. No relevant concomitant medications were reported. She has tested positive for COVID-19 with home test and at the clinic she also tested positive. She has had so many medical problems to include kidney stones and gastric issues. She has been in since 2017 with stage III for Colorectal Cancer. She was diagnosed in Nov 2017. She had surgery in April 2018 after radiation and a month of those treatments together. No treatment information was provided. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in.; Sender's Comments: Company comment: This is a spontaneous case concerning a 77-year-old female patient with Colorectal cancer stage III on treatment with encorafenib and erbitux, who experienced the unexpected non-serious AESI COVID-19 and the serious event nephrolithiasis. More than four months after receiving the booster dose of mRNA-1273, patient was tested positive twice and reported had no symptoms of COVID-19. Start date, clinical findings, diagnostic tests and treatment details regarding nephrolithiasis were not provided. Innappropriate schedule of product administration was also captured as an event. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220208; Test Name: SARS-CoV-2 test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Colorectal cancer stage III
- Vorgeschichte
- -
- Andere Medikamente
- (BRAFTOVI); (ERBITUX)
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 17.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Therapeutic response unexpected
Symptomtext
I had a lot of energy after my 2 shots, I was cleaning my house like crazy; No adverse event; This spontaneous case was reported by a patient and describes the occurrence of THERAPEUTIC RESPONSE UNEXPECTED (I had a lot of energy after my 2 shots, I was cleaning my house like crazy) and NO ADVERSE EVENT (No adverse event) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. Patient had no allergies. Patient never had COVID positive test or diagnosis. Patient did not receive other vaccines given within 1 month Prior to Moderna COVID-19 vaccine. On 17-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On an unknown date, the patient experienced THERAPEUTIC RESPONSE UNEXPECTED (I had a lot of energy after my 2 shots, I was cleaning my house like crazy) and NO ADVERSE EVENT (No adverse event). At the time of the report, THERAPEUTIC RESPONSE UNEXPECTED (I had a lot of energy after my 2 shots, I was cleaning my house like crazy) and NO ADVERSE EVENT (No adverse event) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. Patient was not on any concomitant medications for any condition. It was reported that, the patient had a lot of energy for 2-3 days after the dose and got a lot of house cleaning done at that time. Patient believes more in herbal remedies than medications. No treatment medications were provided. This case was linked to MOD-2022-647612 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient had no allergies. Patient never had COVID positive test or diagnosis. Patient did not receive other vaccines given within 1 month prior to Moderna COVID-19 vaccine.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 20.08.2021
- Beginn
- 23.08.2022
- Tage bis Beginn
- 368,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; fully vaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 8/23/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Hypertension
- Andere Medikamente
- unknown
- Allergien
- hydrocodone, cephalexin monohydrate
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 18.08.2022
- Impfdatum
- 15.11.2021
- Beginn
- 29.07.2022
- Tage bis Beginn
- 256,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt tested positive for COVID on 07/29/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 15.08.2022
- Impfdatum
- 13.10.2021
- Beginn
- 13.08.2022
- Tage bis Beginn
- 304,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Vaccine breakthrough infection
Symptomtext
Breakthrough case COVID-19 after fully vaccinated with three doses of mRNA vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 30.12.2020
- Beginn
- 10.01.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Computerised tomogram
Deafness neurosensory
Deafness unilateral
Magnetic resonance imaging
Viral infection
Symptomtext
Sensorineural hearing loss right ear, 4 times. Hearing loss occured again after contracting actual virus.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram
- Hospital-Tage
- -
- Labordaten
- CT, MRI, Surgical Steroid Injection
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 11.09.2021
- Beginn
- 12.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Movement disorder
Symptomtext
The following day after my second dose of the Moderna vaccine, I experienced numbness and limited movement on the right side of my face. I had Bells Palsy in my teens and it felt similar to that but cleared up by the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- N/A - I am only reporting this now because I am being asked about doing a follow up dose for booster by my employer and I do not feel comfortable doing an additional doses for fear of developing Bells Palsy again.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.06.2022
- Impfdatum
- 09.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
SARS-CoV-2 test
Suspected COVID-19
Symptomtext
possibly caught the virus/ Tested but don't have the results back; This spontaneous case was reported by a patient and describes the occurrence of SUSPECTED COVID-19 (possibly caught the virus/ Tested but don't have the results back) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 026L21B, 048F21A and 939902) for COVID-19 vaccination. No Medical History information was reported. On 09-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 28-Feb-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced SUSPECTED COVID-19 (possibly caught the virus/ Tested but don't have the results back). At the time of the report, SUSPECTED COVID-19 (possibly caught the virus/ Tested but don't have the results back) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 31-May-2022, SARS-CoV-2 test: results are pending (Inconclusive) Tested but don't have the results back. No concomitant medications were reported. No treatment details were reported. Patient reported that two other things came back (negative) and was still waiting on COVID test results. Head felled like it was blown off shoulders Company Comment: This is a spontaneous case concerning a patient of an unknown age and gender with no medical history reported, who experienced the unexpected non-serious adverse event of special interest Suspected COVID-19, described as possibly caught the virus, in the context of the third/booster dose of mRNA-1273 vaccine. Latency cannot be properly assessed since event onset date was not provided. Patient had received 2-dose primary series of mRNA-1273 vaccine with no reported adverse event, given at an interval of 28 days which falls within the recommended vaccine dosing schedule, approximately 5 months and 3 weeks prior to third mRNA-1273 vaccination. The patient also had head discomfort which described as head feels like it was blown off the shoulders. Patient underwent SARS-CoV-2 test, however, result was not available. No further details about the treatments were provided. Outcome of the event Suspected COVID-19 was unknown. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This is a spontaneous case concerning a patient of an unknown age and gender with no medical history reported, who experienced the unexpected non-serious adverse event of special interest Suspected COVID-19, described as possibly caught the virus, in the context of the third/booster dose of mRNA-1273 vaccine. Latency cannot be properly assessed since event onset date was not provided. Patient had received 2-dose primary series of mRNA-1273 vaccine with no reported adverse event, given at an interval of 28 days which falls within the recommended vaccine dosing schedule, approximately 5 months and 3 weeks prior to third mRNA-1273 vaccination. The patient also had head discomfort which described as head feels like it was blown off the shoulders. Patient underwent SARS-CoV-2 test, however, result was not available. No further details about the treatments were provided. Outcome of the event Suspected COVID-19 was unknown. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220531; Test Name: COVID-19 test; Test Result: Inconclusive ; Result Unstructured Data: Tested but don't have the results back
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.06.2022
- Impfdatum
- 25.08.2021
- Beginn
- 11.05.2022
- Tage bis Beginn
- 259,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Symptomtext
Took Paxlovid on day 1 of being positive; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (Took Paxlovid on day 1 of being positive) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. Concurrent medical conditions included Drug allergy (No, unknown historical drug.). Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) for an unknown indication. On 25-Aug-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-May-2022, the patient experienced COVID-19 (Took Paxlovid on day 1 of being positive). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 11-May-2022 to 15-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. In May 2022, COVID-19 (Took Paxlovid on day 1 of being positive) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 11-May-2022, SARS-CoV-2 test: positive (Positive) Positive. In May 2022, SARS-CoV-2 test: negative (Negative) Negative and positive (Positive) Positive. It was reported that patient symptoms returned on Day 12. Patient thought they were allergies. Patient tested positive again for COVID 19 on day 16. The patient had received any other medications/products within 2 weeks of starting COVID-19 treatment. The patient had previously receive a COVID-19 Vaccine. Device Date reported as 26-May-2022 Company comment: This spontaneous case concerns a patient of unknown age and gender with no relevant medical history who experienced the unexpected non serious of COVID 19 which occurred approximately 9 months after the administration of third dose of mRNA-1273 vaccine in COVID 19 vaccination series. Patient received NIRMATRELVIR, RITONAVIR (Paxlovid) as treatment for COVID 19 from 11-May to 15-May. Patient tested negative 7 days after testing positive. Symptoms returned on day 12 and patient tested positive again for COVID 19. The benefit-risk relationship of mRNA-1273 is not affected by this report. Sender's Comments: This spontaneous case concerns a patient of unknown age and gender with no relevant medical history who experienced the unexpected non serious of COVID 19 which occurred approximately 9 months after the administration of third dose of mRNA-1273 vaccine in COVID 19 vaccination series. Patient received NIRMATRELVIR, RITONAVIR (Paxlovid) as treatment for COVID 19 from 11-May to 15-May. Patient tested negative 7 days after testing positive. Symptoms returned on day 12 and patient tested positive again for COVID 19. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220511; Test Name: COVID-19 virus test; Test Result: Positive; Result Unstructured Data: Positive; Test Date: 202205; Test Name: COVID-19 virus test; Test Result: Negative; Result Unstructured Data: Negative; Test Date: 202205; Test Name: COVID-19 virus test; Test Result: Positive; Result Unstructured Data: Positive.
- Aktuelle Erkrankungen
- Drug allergy (No, unknown historical drug.)
- Vorgeschichte
- -
- Andere Medikamente
- SYNTHROID.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 21.09.2021
- Beginn
- 25.05.2022
- Tage bis Beginn
- 246,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 5,0
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 20.11.2021
- Beginn
- 19.03.2022
- Tage bis Beginn
- 119,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Herpes zoster
Menstruation irregular
Oligomenorrhoea
Symptomtext
My very first dose of the COVID-19 vaccine was J&J. My first and second booster vaccine was Moderna. After receiving both Moderna vaccines, I experienced shingles about 4 months later. The main area for the shingles was my lower, left back/hip. I am currently 5-6 weeks into having them on my body. They are manageable at this time. I received anti-viral medication from the minute clinic and I had it confirmed by my PCP. I also experienced a change in my menstrual cycles after receiving my second Moderna booster. I have always had regular cycles (8 days), but now I experience a cycle of 12 days. This has occurred the past 5 months after receiving my booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- I did not have any tests completed.
- Aktuelle Erkrankungen
- I was not experiencing any illness.
- Vorgeschichte
- I have skin contact Dermatitis; High Blood Pressure.
- Andere Medikamente
- I was taking Chlorthalidone 25mg; Vitamin D; Pramipexole 0.125mg.
- Allergien
- I am allergic to all adhesives (like Band-Aids); Chlorohexidine.
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 23.03.2022
- Impfdatum
- 04.10.2021
- Beginn
- 03.02.2022
- Tage bis Beginn
- 122,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
Patient was hospitalized with COVID after receiving COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 01.09.2021
- Beginn
- 24.01.2022
- Tage bis Beginn
- 145,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID on Jan 24, 2022, developed bronchitis on Jan 27,2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Eosinophilic asthma
- Andere Medikamente
- Breztri, Dupixent, metroprolol, spironolactone, estradiol, vitamin D, once a day vitamin, Benadryl, Claritin,
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired Vaccine administered to patient; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient) in a 21-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 01-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Aug-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient). On 01-Aug-2021, EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient) to be possibly related. No concomitant medication details was reported. No treatment medication details was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired Vaccine administered to patient; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 01-Aug-2021 at 12:16 PM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient). On 01-Aug-2021, EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Additional information provided for vaccine that was punctured on 31-JUL-2021 and was kept at room temperature of 67.2 Fahrenheit for 11 hours and 15 minutes beyond the punctured vial 12 hour expiration before administration to the patient. Concomitant product use was not provided. Treatment information was not provided. This case was linked to MOD-2021-273049, MOD-2021-273129, MOD-2021-273149, MOD-2021-273448, MOD-2021-273721 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired Vaccine administered to patient; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient) in a 36-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 01-Aug-2021 at 10:50 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient). On 01-Aug-2021, EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was provided No treatment medication was provided 1 Vial of Moderna COVID-19 vaccine was taken out of the refrigerator, punctured and kept at room temperature (67.2F) beyond 12 hours. The vial was first punctured at 1:01PM on 31-Jul-2021 and that is when it was first moved to the room temperature. Punctured Vial kept in room temperature beyond 12 hours.Total amount of time the punctured vial was exposed to room temperature range: 9 hours and 49 minutes at 67.2 Fahrenheit steady temperature This case was linked to MOD-2021-273049 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired Vaccine administered to patient; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient) in a 30-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 01-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Aug-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient). On 01-Aug-2021, EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered to patient) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant Medications were provided. No treatment information was provided. One vial of Moderna COVID-19 vaccine was taken out of the refrigerator, punctured and kept at room temperature (67.2F) beyond 12 hours. The vial was first punctured at 1:01PM on 31JUL2021 and that is when it was first moved to the room temperature.Patient number four received his first dose of Moderna COVID-19 Vaccine on 01AUG2021 at 11:27AM (10 hours and 26 minutes beyond punctured vial 12 hour expiration at room temperature). This case was linked to MOD21-125492, MOD21-125573, MOD21-125575, MOD21-125577, and MOD21-125580, MOD-2021-273049 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 24.08.2021
- Beginn
- 20.01.2022
- Tage bis Beginn
- 149,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough of COVID after being vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test positive
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Fibromyalgia
- Andere Medikamente
- Cymbalta; Premarin
- Allergien
- Codeine; amoxicillin; Fragmin; Lortab; Micovib
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 08.10.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Biopsy bone marrow
Blood test
Thrombocytopenia
Symptomtext
THROMBOCYTOPENIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy bone marrow
- Hospital-Tage
- 4,0
- Labordaten
- BLOOD WORK BONE MARROW BIOPSY
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- MS
- Andere Medikamente
- acyclovir vitaminD 50000 olmesartan modafinil
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 20.02.2022
- Impfdatum
- 14.09.2021
- Beginn
- 21.01.2022
- Tage bis Beginn
- 129,0
- Dosis
- 2
- Route/Site
- - / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Symptomtext
Shingles developed on front and back torso. Initial Treatment: Medro Pak 4mcg 6 days, Acyclorir 400 mcg 7 days,Tramadol 50 50 mg 10 days. Second Treatment upon second visit ; Gabapentin 300 mg daily for 30 days with 2 refills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- vitamin D3 50 MCG 1/day; Losartan 50 MCG 2/day; Hydroclorothazmide 1/day
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 12.01.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 360,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Received Aug 2021 and contracted Covid January 2022, lasted for a month and only saw doctor through video exam.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamin, Calcium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 17.02.2022
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Gave client booster dose instead of 3rd dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Vaccine in a vial punctured more than 12 hours ago and improperly stored administered to 3; Vaccine in a vial punctured more than 12 hours ago and improperly stored administered to 3; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine in a vial punctured more than 12 hours ago and improperly stored administered to 3) and PRODUCT STORAGE ERROR (Vaccine in a vial punctured more than 12 hours ago and improperly stored administered to 3) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 14-Oct-2021 at 9:19 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine in a vial punctured more than 12 hours ago and improperly stored administered to 3). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine in a vial punctured more than 12 hours ago and improperly stored administered to 3). On 14-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Vaccine in a vial punctured more than 12 hours ago and improperly stored administered to 3) had resolved. At the time of the report, PRODUCT STORAGE ERROR (Vaccine in a vial punctured more than 12 hours ago and improperly stored administered to 3) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. No other adverse reactions that reporter was aware of.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Vaccine in a vial punctured more than 12 hours ago administered; Vaccine in a vial improperly stored; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine in a vial punctured more than 12 hours ago administered) and PRODUCT STORAGE ERROR (Vaccine in a vial improperly stored) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 23-Sep-2021 at 2:20 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine in a vial punctured more than 12 hours ago administered) and PRODUCT STORAGE ERROR (Vaccine in a vial improperly stored). On 23-Sep-2021, EXPIRED PRODUCT ADMINISTERED (Vaccine in a vial punctured more than 12 hours ago administered) and PRODUCT STORAGE ERROR (Vaccine in a vial improperly stored) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant products were reported. No other adverse reactions were reported. No treatment information was reported. Most recent FOLLOW-UP information incorporated above includes: On 01-Feb-2022: Follow-up received contains patient identifiers, dose number, administration site details added and narrative updated (No adverse reaction).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 05.08.2021
- Beginn
- 08.01.2022
- Tage bis Beginn
- 156,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Got the booster dose too early, because of the negligence of the pharmacist. It was 24 days before the 5 months; This spontaneous case was reported by a consumer and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Got the booster dose too early, because of the negligence of the pharmacist. It was 24 days before the 5 months) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 033H21A, 037F21A and 939902) for COVID-19 vaccination. No Medical History information was reported. On 05-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Jan-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Jan-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Got the booster dose too early, because of the negligence of the pharmacist. It was 24 days before the 5 months). On 08-Jan-2022, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Got the booster dose too early, because of the negligence of the pharmacist. It was 24 days before the 5 months) had resolved. No concomitant medications were reported. No treatment medications were reported. The reporter denied side effects. It was reported that there was no product complaint associated with this case. This case was linked to MOD-2022-467290, MOD-2022-467313 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 26.08.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
dose administered after 30-day Use by Date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (dose administered after 30-day Use by Date) in a 42-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 939902 and 939902) for COVID-19 vaccination. No Medical History information was reported. On 26-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 23-Sep-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (dose administered after 30-day Use by Date). On 23-Sep-2021, EXPIRED PRODUCT ADMINISTERED (dose administered after 30-day Use by Date) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported 2nd dose was stored on the refrigerator since 10 Aug 2021. No concomitant medications details were reported. No treatment information details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 05.11.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Electrocardiogram
Heart rate increased
Symptomtext
Atrial fibrillation and fast hearbeat detected on EKG on January 7. Cardiology nurse said it could be related to vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- EKG on January 7. Cardiology nurse said onset of atrial fibrillation and fast heartbeat could be related to vaccine.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- magnesium glycinate, coenzyme q10, vitamins c & d
- Allergien
- pumpklin seeds
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 26.09.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 102,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 09.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Blood iron decreased
Blood test
Deafness unilateral
Ear discomfort
Injury
Nerve injury
Symptomtext
1) My left ear began feel very stopped up 3 days after my first vaccine on 8-9-2021. I went to my PCP on 8-19-2021 to have my ears checked. No indication of infection, ordered steroids for 5 days. No change in my ear after the 5 days. 2) Had routine follow up and blood work with my Hematologist on 8-26-2021. His office called me a few days later to report that my iron level had dropped dramatically and he was going to schedule an IV of 3) Second visit to PCP on 12-21-2021 due to continue having issue with left ear, feeling of fullness and seemed to be stopped up. He ordered another round of steroids and antibiotics even though there was no indication of an infection. Meds did not do anything for my ear. iron to be administered. I have not had to have IV iron in almost 5 years and my blood work in June did not indicate any problems with my iron. 4) Made appointment and saw the ENT on 1-6-2022. He examined both ears and performed a hearing test. It was determined that I do not have any pressure in my ear even though it has felt like I do since August 12th of 2021, 3 days after receiving my first COVID vaccine. The ENT advised that this damage is permanent and this hearing loss will not return. 5) The different doctors have advised that I do not receive any further COVID vaccines as the extreme adverse events could have been caused from the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests abnormal
- Hospital-Tage
- -
- Labordaten
- Lab test on 8-26-2021 revealed iron at 7 which is a critical range requiring intervention. Hearing test on 1-6-2021 revealed nerve damage and hearing loss to left ear.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Controlled hypertension, hypothyroidism and iron deficiency anemia
- Andere Medikamente
- Lisinopril, Levothyroxine, Hydrochlorothiazide, Vitamin C, B-12, Vitamin D, Multivitamin, Zyrtec, Baby ASA
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- U
- Eingang
- 31.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Expired product administered
Product storage error
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; 55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture) in a 60-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 03-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture). On 03-Dec-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitants medications was reported. No treatments medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- U
- Eingang
- 31.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 23-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 16-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 16-Dec-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication details were not reported by the reporter. Treatment details was not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- U
- Eingang
- 31.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients received a dose of a vial after 12 hours of initial puncture) in a 34-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 15-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients received a dose of a vial after 12 hours of initial puncture). On 15-Dec-2021, EXPIRED PRODUCT ADMINISTERED (patients received a dose of a vial after 12 hours of initial puncture) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. NO Concomitant drug reported. NO Treatment drug reported Vial puncture on 11 Nov 2021, dose given, kept in refrigerator after puncture. This case was linked to MOD-2021-418964 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Vial puncture 11/11/21dose given kept in refrigerator after puncture; Patient received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (Vial puncture 11/11/21dose given kept in refrigerator after puncture) in a 29-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a dose of a vial after 12 hours of initial puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial puncture 11/11/21dose given kept in refrigerator after puncture). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Patient received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (Vial puncture 11/11/21dose given kept in refrigerator after puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported No treatment information was provided The vial punctured on 11 Nov 2021 dose given kept in refrigerator after puncture.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 64,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 64-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 23-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 23-Nov-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 63-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 19-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 19-Nov-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant information was reported. No treatment information was reported. This case was linked to MOD-2021-418964 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 19-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 19-Nov-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment information was not provided by the reported. This case was linked to MOD-2021-418964 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 29-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant Drug details were reported. No Treatment information was provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 61,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 17.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 61-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 17-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 17-Nov-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information was reported. This case was linked to MOD-2021-418964 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 70-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 12-Nov-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided by the reporter. No treatment information was provided by the reporter. There were two vials that were punctured and used some time between June and November 5, but can't back track those dates, they were written on the vials themselves, which were disposed of. It just came to their attention that the vials were being used past the recommended 12 hour post puncture time. It was reported that vial was punctured on 11-NOV-2021 and dose given then kept in refrigerator after puncture. This case was linked to MOD-2021-418964 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 59,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a dose of a vial after 12 hours of initial puncture) in a 59-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 30-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a dose of a vial after 12 hours of initial puncture). On 30-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Patient received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was reported. No treatment medications were provided. Reporter stated vial was punctured on 11-Nov-2021 and kept in refrigerator after puncture. This case was linked to MOD-2021-418964 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; 55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture) in a 34-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 15-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture). On 15-Dec-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. No treatment information was provided by the reporter. The vial was puncture on 11-Nov-2021, dose given and kept in refrigerator after puncture.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 53-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 16-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 12-Dec-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 19,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 19-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 15-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 15-Dec-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. No treatment medication were provided. Vial was punctured on 11-Nov-2021 and kept in refrigerator after puncture. This case was linked to MOD-2021-418964 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- U
- Eingang
- 25.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 52-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 23-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 23-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 23-Nov-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided by the reporter. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- U
- Eingang
- 24.12.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Expired product administered
Product storage error
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; Improper storage conditions; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (Improper storage conditions) in a 62-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milligram. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (Improper storage conditions). At the time of the report, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (Improper storage conditions) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. No treatment medication was reported. The vial was punctured on 11-Nov-2021, after dose administration, was kept in the refrigerator after puncture.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- U
- Eingang
- 24.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
55 patients received a dose of a vial after 12 hours of initial puncture; 55 patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture) in a 55-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 06-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture). On 06-Dec-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. The vial punctured on 11-Nov-2021, dose given and kept in refrigerator after puncture. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- U
- Eingang
- 24.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture) in a 51-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 03-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture). On 03-Dec-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) and PRODUCT STORAGE ERROR (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided Treatment medication was not provided by the reporter It was reported that the vial puncture on 11/11/21, dose given, kept in refrigerator after puncture
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 24,0
- Geschlecht
- U
- Eingang
- 24.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) in a 24-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 03-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture). On 03-Dec-2021, EXPIRED PRODUCT ADMINISTERED (55 patients received a dose of a vial after 12 hours of initial puncture) had resolved. Not Provided. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Vial was punctured on 11-Nov-21, dose was given, kept in refrigerator after puncture. It was reported that there were two vials that were punctured and used some time between June and 5 -November , but reporter can't back track those dates, they were written on the vials themselves, which were disposed of. It just came to their attention that the vials were being used past the recommended 12 hour post puncture time. No concomitant medication was provided. No treatment medication was provided. This case was linked to MOD-2021-418964 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 41,0
- Geschlecht
- U
- Eingang
- 24.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Expired product administered
Symptomtext
patients received a dose of a vial after 12 hours of initial puncture; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED in a 41-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 30-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED. On 30-Nov-2021, EXPIRED PRODUCT ADMINISTERED had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were reported. No Treatment details were reported. This case was linked to MOD-2021-418964 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 08.09.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 27,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Skin discolouration
Symptomtext
1. On or about October 5, 2021, after driving for approximately 2.5 hours, I could no longer feel my left foot. After moving my left thigh and knee in all directions for about 30 seconds to 1 minute, I began regaining some feeling and sensation in my left foot. I then stopped the vehicle and walked and more feeling returned. Since that episode, similar ones (at least 3 more) have occurred after sitting too long; one of these occurred after a long period of sleep. For 2 of the loss of feeling episodes, I examined the appearance of my left foot and found a disconnected spidery vein pattern in the flat inside of my ankle between the ankle bone and the heel. The patterned area and surrounding were discolored.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- muscle weakness and reduced circulation in lower left leg and left foot
- Andere Medikamente
- tamsulosin (script), multi vitamin, tumeric, resveratrol,
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 15.10.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 64,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Client received Booster of Moderna to early, no signs or symptoms reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- No recent illness
- Vorgeschichte
- MS
- Andere Medikamente
- Client could not remember medication names, she is on medication for MS
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 26.10.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
X-ray
Symptomtext
11/09/2021, 2 weeks post vaccine, My wife had a bad cough. I caught it from her. I went to the doctor he called in a prescription, He gave me Cal syrup and administered a steroid shot, and some type of "cillin" not penicillin, and I also took some steroid pills before I got the shot. And I still have the cough, mostly in the evening. He took x-rays and nothing showed up on that. I have been to the doctor twice and I am going to see him again. 12/13/2021- I still have the cough, but I do not know if it came from the shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- x-rays - were clear
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High Cholesterol; Diabetes
- Andere Medikamente
- Sertraline 2/100 mg od Bupropion hcl 2 /100 mg od Pantoprazole 40 mg oc Loratadine 10 mg od Metformin hcl 500 mg bd Ezetimibe 10 mg od Vitamin D 3 1000 iu od Glipizide 10 mg bd Losartan 50 mg od
- Allergien
- Statin drugs
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 20.09.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 75,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asymptomatic COVID-19
Symptomtext
COVID symptomatic admission
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 07.12.2021
- Impfdatum
- 25.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Diplopia
Magnetic resonance imaging
Symptomtext
double vision / woke up with double vision; This spontaneous case was reported by a consumer and describes the occurrence of DIPLOPIA (double vision / woke up with double vision) in a 50-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 25-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Nov-2021, the patient experienced DIPLOPIA (double vision / woke up with double vision). At the time of the report, DIPLOPIA (double vision / woke up with double vision) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In November 2021, Blood test: normal (normal) Normal. In November 2021, Magnetic resonance imaging: normal (normal) Normal. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product reported by reporter. No treatment medication reported by reporter. Most recent FOLLOW-UP information incorporated above includes: On 03-Dec-2021: Added reporter information. Added patient information. Added lab data information. Added product details. Added onset date and outcome of event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Test Date: 202111; Test Name: Blood tests; Result Unstructured Data: Normal; Test Date: 202111; Test Name: MRI; Result Unstructured Data: Normal.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 03.08.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 113,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
booster given less than 6 months after 2nd dose; This spontaneous case was reported by a pharmacist and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (booster given less than 6 months after 2nd dose) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 018F21A, 048F21A and 939902) for COVID-19 vaccination. No Medical History information was reported. On 03-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 24-Nov-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 24-Nov-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (booster given less than 6 months after 2nd dose). On 24-Nov-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (booster given less than 6 months after 2nd dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant and treatment product use was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 16.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 15,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalization with covid after being fully vaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 12/1/21
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- hypertension, asthma, and type 2 diabetes
- Andere Medikamente
- unknown
- Allergien
- chocolate flavor, orange juice, sulfa
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 30.08.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 51,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
diagnosed and hospitalized with COVID while fully vaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 20.08.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 96,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested Positive for Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 24.10.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Systemic inflammatory response syndrome
Symptomtext
R65.10 - SIRS (systemic inflammatory response syndrome)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Systemic inflammatory response syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product temperature excursion issue
Symptomtext
56 doses administered after temperature excursion; Vaccines went out of range high 3x for a total of 47 minutes and reached a high of 48.7; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (56 doses administered after temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccines went out of range high 3x for a total of 47 minutes and reached a high of 48.7) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (56 doses administered after temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccines went out of range high 3x for a total of 47 minutes and reached a high of 48.7). At the time of the report, EXPIRED PRODUCT ADMINISTERED (56 doses administered after temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccines went out of range high 3x for a total of 47 minutes and reached a high of 48.7) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Vaccines were not punctured at the time of temperature excursion. The beyond use date (BUD) for the vaccine was on 14-Nov-2021. Vaccine was administered on unknown date Nov-2021. Start date for the events was on unknown date Nov-2021 and was recovered on Nov-2021. No concomitant medications were reported No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 09.06.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 23,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Laboratory test
Symptomtext
amenorrhea LMP 7/2/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amenorrhoea
- Hospital-Tage
- -
- Labordaten
- advised RTO for sono and hormonal labs
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- hydroperoxide , cat dander, dust mites
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Dose administered after 30-day Use By Date/gave 81 doses of the Moderna Covid-19 Vaccine after the vials were stored in the refrigerator for 30 days; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/gave 81 doses of the Moderna Covid-19 Vaccine after the vials were stored in the refrigerator for 30 days) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/gave 81 doses of the Moderna Covid-19 Vaccine after the vials were stored in the refrigerator for 30 days). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/gave 81 doses of the Moderna Covid-19 Vaccine after the vials were stored in the refrigerator for 30 days) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Dose administered after 30-day Use By Date / 81 doses of the Moderna Covid-19 Vaccine after the vials were stored in the refrigerator for 30 days; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date / 81 doses of the Moderna Covid-19 Vaccine after the vials were stored in the refrigerator for 30 days) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 26-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date / 81 doses of the Moderna Covid-19 Vaccine after the vials were stored in the refrigerator for 30 days). On 26-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date / 81 doses of the Moderna Covid-19 Vaccine after the vials were stored in the refrigerator for 30 days) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. Reporter reported that Last one was in the refrigerator with a label on it (not to be used in patients). Date the vial was initially stored in the refrigerator was 2Aug2021. On 03-SEP-2021 4 doses were administered. On 20-SEP-2021 4 doses were administered. On 01-OCT-2021 7 doses were administered. On 18-OCT-2021 4 doses were administered. On 25-OCT-2021 19 booster doses were administered. On 26-OCT-2021 14 booster doses were administered. On 27-OCT-2021 19 booster doses were administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Dose administered after 30-day Use By Date/25Oct2021 19 booster doses; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/25Oct2021 19 booster doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 25-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/25Oct2021 19 booster doses). On 25-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/25Oct2021 19 booster doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
they gave 81 doses of the Moderna Covid-19 Vaccine after the vials werestored in the refrigerator for 30 days; they gave 81 doses of the Moderna Covid-19 Vaccine after the vials werestored in the refrigerator for 30 days; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (they gave 81 doses of the Moderna Covid-19 Vaccine after the vials werestored in the refrigerator for 30 days) and EXPIRED PRODUCT ADMINISTERED (they gave 81 doses of the Moderna Covid-19 Vaccine after the vials werestored in the refrigerator for 30 days) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 18-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Oct-2021, the patient experienced PRODUCT STORAGE ERROR (they gave 81 doses of the Moderna Covid-19 Vaccine after the vials werestored in the refrigerator for 30 days) and EXPIRED PRODUCT ADMINISTERED (they gave 81 doses of the Moderna Covid-19 Vaccine after the vials werestored in the refrigerator for 30 days). On 18-Oct-2021, PRODUCT STORAGE ERROR (they gave 81 doses of the Moderna Covid-19 Vaccine after the vials werestored in the refrigerator for 30 days) and EXPIRED PRODUCT ADMINISTERED (they gave 81 doses of the Moderna Covid-19 Vaccine after the vials werestored in the refrigerator for 30 days) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. no concomitant drugs were reported. no treatment drugs were reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Dose administered after 30-day Use By Date/01Oct2021 7 doses; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/01Oct2021 7 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 01-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/01Oct2021 7 doses). On 01-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/01Oct2021 7 doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No Treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.11.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
They gave 81 doses of the Moderna Covid-19 Vaccine (all from lot 939902) after the vials were; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (they gave 81 doses of the Moderna Covid-19 Vaccine (all from lot 939902) after the vials were) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 03-Sep-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (they gave 81 doses of the Moderna Covid-19 Vaccine (all from lot 939902) after the vials were). On 03-Sep-2021, EXPIRED PRODUCT ADMINISTERED (they gave 81 doses of the Moderna Covid-19 Vaccine (all from lot 939902) after the vials were) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Treatment medication was not provided. Concomitant medication was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 05.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Dose administered after 30-day Use By Date/03Sep2021 4 doses; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/03Sep2021 4 doses) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/03Sep2021 4 doses). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date/03Sep2021 4 doses) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided Treatment medications were not provided Reported that 68 doses of the Moderna Covid-19 Vaccine (all from lot 939902) used after the vials were stored in the refrigerator for 30 days.Dose administered after 30-day Use By Date. Date the vial was initially stored in the refrigerator: 02-Aug-2021. Date of vaccine administration was reported as 03 Sep 2021- 4 doses, 20 Sep 2021 -4 doses, 01 Oct 2021- 7 doses,18 Oct 2021 -4 doses , 25 Oct 2021 -19 booster doses, 26 Oct 2021- 14 booster doses, 27 Oct 2021 -19 booster doses. Most recent FOLLOW-UP information incorporated above includes: On 28-Oct-2021: Follow up received on 28-Oct-2021 contains: Date(s) of administration of vaccine added and updated in I narrative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 31.08.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BEYOND USE DATE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BEYOND USE DATE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BEYOND USE DATE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BEYOND USE DATE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BEYOND USE DATE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Device use issue
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Device use issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. VACCINE ADMINSTERED PAST BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 03.09.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
NO ADVERSE EVENT OCCURED. ADMINISTERED VACCINE AFTER BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 15.09.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 38,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heavy menstrual bleeding
Symptomtext
Heavy menstruation after 17+ years of only spotting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension, diabetes
- Andere Medikamente
- Benazapril/HCTZ, Metformin, lovastatin
- Allergien
- Sulfa, wine, beer
- Vorherige Impfungen
- COVID arm, COVID-19 Vac Moderna, 2/5/21; 3/5/21